This Consensus Statement summarizes recommendations for clinical diagnosis, investigation and management of patients with Silver–Russell syndrome (SRS), an imprinting disorder that causes prenatal and postnatal growth retardation. Considerable overlap exists between the care of individuals born small for gestational age and those with SRS. However, many specific management issues exist and evidence from controlled trials remains limited. SRS is primarily a clinical diagnosis; however, molecular testing enables confirmation of the clinical diagnosis and defines the subtype. A 'normal' result from a molecular test does not exclude the diagnosis of SRS. The management of children with SRS requires an experienced, multidisciplinary approach. Specific issues include growth failure, severe feeding difficulties, gastrointestinal problems, hypoglycaemia, body asymmetry, scoliosis, motor and speech delay and psychosocial challenges. An early emphasis on adequate nutritional status is important, with awareness that rapid postnatal weight gain might lead to subsequent increased risk of metabolic disorders. The benefits of treating patients with SRS with growth hormone include improved body composition, motor development and appetite, reduced risk of hypoglycaemia and increased height. Clinicians should be aware of possible premature adrenarche, fairly early and rapid central puberty and insulin resistance. Treatment with gonadotropin-releasing hormone analogues can delay progression of central puberty and preserve adult height potential. Long-term follow up is essential to determine the natural history and optimal management in adulthood.
Silver–Russell syndrome (SRS, OMIM #180860, also known as Russell–Silver syndrome, RSS) is a rare, but well-recognized, condition associated with prenatal and postnatal growth retardation. The syndrome was first described by Silver et al.1 and Russell2, who independently described a subset of children with low birth weight, postnatal short stature, characteristic facial features and body asymmetry. Almost all patients with SRS are born small for gestational age (SGA; Box 1). The aetiology of intrauterine growth retardation and SGA is extremely heterogeneous. Children with SRS can be distinguished from those with idiopathic intrauterine growth retardation or SGA and postnatal growth failure by the presence of other characteristic features, including relative macrocephaly (defined as a head circumference at birth ≥1.5 SD score (SDS) above birth weight and/or length SDS), prominent forehead, body asymmetry and feeding difficulties3,4,5,6.
Globally, estimates of the incidence of SRS range from 1:30,000 to 1:100,000 (Ref. 7). In 2015, a study in Estonia8 estimated an incidence of 1:70,000; however, only molecularly confirmed cases were included, which could have resulted in underdiagnosis. Overall, SRS is probably more common than some previous estimates have suggested, but the exact incidence remains unknown.
An underlying molecular cause can currently be identified in around 60% of patients clinically diagnosed with SRS4. The most common underlying mechanisms are loss of methylation on chromosome 11p15 (11p15 LOM; seen in 30–60% of patients) and maternal uniparental disomy for chromosome 7 (upd(7)mat; seen in ∼5–10% of patients)4,9,10. However, the molecular aetiology remains unknown in a substantial proportion of patients.
Although considerable overlap exists in the clinical care of individuals born SGA and those with SRS, many management issues are specific to SRS. These include notable feeding difficulties, severe postnatal growth failure with no catch-up, recurrent hypoglycaemia, premature adrenarche, fairly early and rapid central puberty, insulin resistance and body asymmetry. Identification of the molecular cause in many patients has also raised questions about the management of individual molecular subtypes of SRS. As evidence from controlled trials is limited, a consensus meeting was organized to develop guidelines for the diagnosis and management of patients with SRS.
This Consensus Statement was produced on behalf of the COST Action BM1208 (European Network for Human Congenital Imprinting Disorders, http://www.imprinting-disorders.eu), European Society of Pediatric Endocrinology (ESPE), Pediatric Endocrine Society (PES), Asian Pacific Pediatric Endocrine Society (APPES) and Sociedad Latino-Americana de Endocrinología Pediátrica (SLEP).
41 task force members from 16 countries, chosen for their publication record and expertise in SRS, collaborated to develop this consensus statement. They included paediatric endocrinologists, clinical geneticists, molecular geneticists, a gastroenterologist and five non-voting representatives from a parent support group. Participants included representatives nominated by the council and clinical practice committees from four international paediatric endocrine societies. All participants signed a conflict of interest declaration, and the consensus was supported by academic funding, without pharmaceutical support. A Delphi-like consensus methodology was adopted11. A comprehensive literature search was conducted using PubMed and the search terms “Silver Russell syndrome” and “Russell Silver syndrome”. Additional relevant articles on SGA, differential diagnoses and growth hormone (GH) were also identified by PubMed searches when supplementary information was necessary. A comprehensive review of >600 articles formed the basis of discussion by three working groups. These groups focused on clinical diagnosis (working group 1: E.L.W., J.S., K.H.C., M.E., R.P.D., P.G.M., T.O., E.S., M.T. and I.K.T.), molecular testing (working group 2: F.B., J.B., K.G., M.K., D.M., G.E.M., S.R., Z.T., T.E. and D.J.G.M) and clinical management (working group 3: O.L.-S., S.M.O'C., J.H.D., A.P.M.C., B.D., E.G., A.G., A.C.S.H.-K., A.A.J., A.L., M.M., K.M., I.O.P., G.B., M.D.H. and I.N.), with 10, 10 and 16 members, respectively. Preparations for the consensus took place over 10 months, including two preparatory meetings and regular teleconference discussions between the working group members. At the final consensus meeting, propositions and recommendations were considered by participants and discussed in plenary sessions, enabling reformulation of the recommendations if necessary. Where published data were unavailable or insufficient, experts' clinical experiences and opinions were considered. Finally, all experts voted on the recommendations of each working group using the following system:
Evidence or general agreement allow full agreement with the recommendation
Evidence or general agreement are in favour of the recommendation
Evidence or general agreement are weak for the recommendation
There is not enough evidence or general agreement to agree with the recommendation
Depending on the proportion of votes received, the strength of the recommendation was recorded as follows:
+ 26–49% of the votes
++ 50–69% of the votes
+++ ≥70% of the votes
SRS is currently a clinical diagnosis based on a combination of characteristic features. Molecular testing can confirm the diagnosis in around 60% of patients4. Molecular testing enables stratification of patients with SRS into subgroups, which can lead to more tailored management. However, molecular investigations are negative in a notable proportion of patients with characteristic clinical features of SRS. For these patients, an established clinical diagnosis enables access to appropriate support groups, treatment (including GH) and further research into the underlying incidence, natural history and aetiology of the SRS phenotype.
However, the diagnosis of SRS can be difficult, as the condition varies widely in severity among affected individuals and many of its features are nonspecific4,5,6. Until now, no consensus has been reached on the clinical definition of SRS. Historically, this lack of consensus has probably led to underdiagnosis and overdiagnosis, particularly by clinicians unfamiliar with SRS.
Several clinical scoring systems for SRS have been proposed, which reflects the challenge in reaching a confident diagnosis4,5,12,13,14,15. All the systems use similar criteria, but vary in the number and definition of diagnostic features required for diagnosis. The relative sensitivity and specificity of these scoring systems have been compared in patients with confirmed molecular diagnoses14,15.
Netchine–Harbison clinical scoring system
The Netchine–Harbison clinical scoring system (NH-CSS; Table 1), which was proposed by Azzi and colleagues in 2015,15 is the only scoring system for the diagnosis of SRS that was developed using prospective data. Four of the six criteria are objective; protruding forehead and feeding difficulties remain subjective, but clear clinical definitions are given. Using the same cohort, the NH-CSS proved more sensitive (98%) than previous systems4,14. The NH-CSS also had the highest negative predictive value (89%), which gives a high degree of confidence that patients who have less than four of the six clinical criteria for diagnosis are truly unaffected by SRS. The system is easy to use in a busy clinical setting. The NH-CSS is also flexible enough to use even if data are incomplete, which is important as the diagnosis is often made in infancy, before information about postnatal growth and BMI is available.
Similarly to other clinical scoring systems, the NH-CSS has a low specificity (36%)15, which could result in false positive results when the diagnosis is just based on clinical findings. Relative macrocephaly at birth (defined as a head circumference at birth ≥1.5 SDS above birth weight and/or length SDS) and protruding forehead are the two features in the NH-CSS that best distinguish SRS from non-SRS SGA (see Supplementary information S1 (table))4,15,16,17,18. To maintain confidence in the clinical diagnosis if all molecular testing is normal, we recommend that only patients scoring at least four of six criteria, including both prominent forehead and relative macrocephaly, should be diagnosed as 'clinical SRS' (previously known as 'idiopathic SRS'); see the flow diagram for investigation and diagnosis of SRS (Fig. 1).
Diagnosis in late childhood or adulthood
All scoring systems for SRS have been developed and validated in paediatric cohorts. However, an increasing number of adults with a historical diagnosis of SRS are being seen by clinicians, particularly regarding their concerns about passing the condition on to their offspring (personal experience of working groups 1 and 3). In these patients, a clinical diagnosis is frequently challenged by lack of early growth data. An attempt should be made to obtain photographs of the individual aged 1–3 years, especially of the face in profile, as well as measurements at birth and in the first 2 years. No current evidence exists to support an alternative approach to diagnosis in adults.
Additional clinical features
In addition to the clinical features in the NH-CSS, several others are recognized in association with SRS, as shown in Table 2 and Supplementary information S1 (table). These characteristics are not specific to SRS, and might be present in children born SGA who do not have SRS, but at a lower frequency than in patients with SRS. However, a few features occur at a much higher rate in children with SRS than in those with SGA4,15,16. These features include low muscle mass, crowded or irregular teeth, micrognathia, down-turned mouth, clinodactyly and excessive sweating.
1.1 SRS should remain primarily a clinical diagnosis. Molecular testing is useful for the confirmation and stratification of diagnosis in SRS. Lack of a positive molecular result does not exclude the diagnosis of SRS. (A+++)
1.2 The flow chart (Fig. 1), based on the NH-CSS, should be adopted for the investigation and diagnosis of SRS. (A++)
1.3 In children aged <2 years, adolescents and adults, a reduced threshold for molecular testing might be required due to missing data. (A++)
Investigation and diagnosis
A positive molecular test result provides useful confirmation of the clinical diagnosis (Fig. 1). This result also enables stratification into a specific molecular subgroup that, in turn, can help guide appropriate management. However, many patients are referred for molecular testing with few, or atypical, features of SRS, which leads to low diagnostic yields and incurs unnecessary expense19. We, therefore, recommend the use of the flow chart in Fig. 1 to aid in the investigation and diagnosis of SRS.
Some patients, particularly those with upd(7)mat, have fewer typical clinical features of SRS than patients with 11p15 LOM4,5,13,16,20,21. In the cohort reported by Azzi and co-workers15, one of the nine patients scoring three of six criteria (and therefore predicted 'unlikely to have SRS') had upd(7)mat. The threshold recommended in Fig. 1 for molecular testing (≥3 of six criteria) is, therefore, lower than that needed for a clinical diagnosis of SRS (≥4 of six criteria).
Conversely, in the same cohort, no positive molecular diagnoses were made in patients scoring less than three of six criteria15. Other studies have also excluded 11p15 LOM and upd(7)mat in patients born SGA with postnatal growth retardation but without additional features of SRS4,10,22. We, therefore, do not recommend testing for SRS in patients scoring less than three of six criteria. Of note, a small number of patients with body asymmetry have been reported to have 11p15 LOM without associated growth retardation, probably due to tissue mosaicism20,21,23. These patients would score fewer than three of six criteria, which is insufficient to justify a clinical diagnosis of SRS in these patients.
Both SRS and the overgrowth condition Beckwith–Wiedemann syndrome are associated with molecular abnormalities of chromosome 11p15.5, which contains two imprinted domains (Fig. 2). Imprinting of the telomeric domain, which is strongly implicated in SRS24,25, is controlled by the paternally methylated imprinting control region H19/IGF2 IG-DMR (H19/IGF2 intergenic differentially methylated region, previously known as IC1, ICR1 and H19 DMR). The centromeric domain contains the maternally expressed growth repressor CDKN1C; the imprinting of this gene is controlled by the maternally methylated imprinting control region KCNQ1OT1 TSS-DMR (previously known as IC2, ICR2, LIT1 or KvDMR1). Figure 3 summarises the more common molecular changes at chromosome 11p15 associated with SRS. Hypomethylation of the H19/IGF2 IG-DMR results in reduced paternal IGF2 expression and increased maternal H19 expression, which leads to growth restriction9. Numerous copy number variants (CNVs) involving the 11p15.5 region have been reported; the phenotype is dependent on CNV size, location and parental origin24,26 (see Supplementary information S2 (table)).
Molecular testing must robustly and accurately measure DNA methylation of CpG dinucleotides at H19/IGF2 IG-DMR27. Assays involve either bisulfite analysis28,29,30 or enzymatic methods, such as methylation-specific multiplex ligation-mediated PCR amplification (MS-MLPA) or Southern blotting9,31. The most common test in diagnostic use is MS-MLPA, which is economical on DNA, cost-effective and enables parallel analysis of copy number and DNA methylation31,32. Hypomethylation of H19/IGF2 IG-DMR is frequently incomplete and low levels of hypomethylation might elude detection. Methylation patterns might vary between different tissues and cells (leucocytes, samples from a buccal swab and skin fibroblasts)21,33,34 and could explain cases of a negative molecular diagnosis using a blood sample.
Although copy number change can be detected by MS-MLPA, additional array analysis is useful for characterizing the size and gene content of any CNV identified.
Of individuals with SRS, ≤10% have upd(7)mat35,36. The SRS phenotype of upd(7)mat is thought to result from altered expression of an imprinted growth-regulatory gene (or genes)37. In addition, the duplication of pre-existing pathogenic mutations by isodisomy can lead to the clinical expression of recessive disorders (such as cystic fibrosis) in patients with upd(7)mat38,39,40.
Candidate SRS regions have been suggested through identification of patients with segmental upd(7)mat or CNVs (see Supplementary information S3 (table)); the primary candidate SRS genes on chromosome 7 are currently GRB10 (7p12.1) and MEST (7q32)41,42,43,44,45,46,47,48.
Microsatellite analysis was the first diagnostic test for upd(7)mat35,36; however, this analysis cannot detect imprinting defects (epimutations) and requires DNA from at least one parent. DNA methylation analysis, including at least the imprinting control regions GRB10 alt-TSS-DMR and MEST alt-TSS-DMR, can identify upd(7)mat, epimutations, CNVs and segmental or whole-chromosome variations. DNA methylation analysis, for example by MS-MLPA, is economical on DNA, cost-effective and compatible with parallel analysis of 11p15 (Refs 30,49,50).
If testing of both 11p15 and chromosome 7 is negative, additional molecular testing can be considered.
CNVs. Over 30 different pathogenic CNVs have been described in patients with suspected SRS15,51,52,53. Patients with these CNVs usually have more severe developmental delay and/or intellectual disability than is typically seen in SRS52,53. Some patients fulfil the NH-CSS for diagnosis; others either do not meet the NH-CSS criteria, or insufficient data are given to use the criteria for their assessment. Although features of SRS can be present in individuals with a pathogenic CNV, clinical diagnosis of SRS is not helpful in these cases and management needs to be tailored specifically to the phenotypic consequences of the individual CNV.
While either array comparative genomic hybridization or single nucleotide polymorphism array can be used to detect CNVs, single nucleotide polymorphism array can also detect regions of segmental isodisomy54.
Chromosome 14q32 abnormalities. Molecular abnormalities at the paternally methylated imprinted locus on chromosome 14q32 include upd(14)mat, paternal microdeletions and hypomethylation of the DLK1/GTL2 IG-DMR (also referred to as MEG3-DMR, 14q32 DMR or IG-DMR). These result in Temple syndrome, which has clinical overlap with SRS55,56, including being born SGA, postnatal growth retardation, hypotonia, delay in the development of motor skills and early puberty55.
In cohorts of patients with SRS, a small number of patients have been found to have Temple syndrome: 1 of 127 patients57, 2 of 85 patients56 and 1 of 26 patients15. However, the true incidence of 14q32 abnormalities in patients meeting the NH-CSS criteria for diagnosis remains unknown.
upd(20)mat and upd(16)mat. Patients with both upd(20)mat and upd(16)mat have occasionally been detected among cohorts of patients investigated for prenatal and postnatal growth failure or SRS15,57,58. However, in a study published in 2015, none of eight patients with upd(20)mat had relative macrocephaly or asymmetry59, two important criteria of the NH-CSS, which means that these patients might have eluded formal clinical diagnosis of SRS.
CDKN1C and IGF2 mutations. CDKN1C and IGF2 are the coding genes on chromosome 11p15 that are responsible for the growth anomalies in SRS and Beckwith–Wiedemann syndrome. Maternally transmitted SRS was described in a four-generation family with a CDKN1C gain-of-function mutation60, and paternally transmitted SRS in a family with an IGF2 loss-of-function mutation61. However, no additional mutations have been reported to date in sporadic or familial cases of SRS60,62,63. Sequence analysis of either gene might be considered, particularly in familial cases of SRS where the inheritance pattern is consistent; however, coding variants in these genes are rare60,62,63.
Multi-locus imprinting disturbance. A significant proportion (15–38%) of individuals with 11p15 LOM have multi-locus imprinting disturbance (MLID)33,57,64,65,66. High-density methylation arrays have revealed methylation changes involving both (maternally and paternally) imprinted and non-imprinted loci67,68. However, despite welcome advances in genome-wide methylation screening67,69,70, standardization is required to ensure accurate description of MLID and comparison between cohorts.
The effect of MLID on clinical phenotype remains unclear. No difference in growth parameters was found at birth or at 2 years of age between patients with 11p15 LOM with and without MLID64. Although developmental delay and congenital anomalies were reported in patients with MLID, this finding might have been affected by ascertainment bias57.
Overall, the effect of MLID on clinical phenotype and its relevance for genetic counselling remain uncertain. Further information is needed before recommending testing for MLID outside the research setting.
2.1 Molecular genetic testing should be performed by a health professional experienced in the field of imprinting disorders. Consistent and logical nomenclature should be adopted in publications and in test reporting. (A+++)
2.2 First-line molecular testing should include DNA methylation analysis of the H19/IGF2 IG-DMR and KCNQ1OT1 TSS-DMR. (A+++)
2.3 First-line molecular testing should include analysis of DNA methylation at the GRB10 alt-TSS-DMR and the MEST alt-TSS-DMR. (A+++)
2.4 In case of a positive test result at either 11p15 or chromosome 7, discrimination between epimutation, CNV and upd should be considered to estimate recurrence risk. (A+++)
2.5 After exclusion of changes in 11p15 and chromosome 7, a clinical decision should be sought about the direction of further testing. Depending on the clinical features and family history of the patient, further testing might include CNV analysis and DNA methylation analysis at chromosome 14q32. Testing might also be considered for very rare molecular anomalies, including upd(20)mat, upd(16)mat and mutations in CDKN1C and IGF2, as well as analysis of further tissues to detect somatic mosaicism. (A++)
2.6 When an underlying pathogenic CNV is identified, the diagnosis should focus on this finding, even if features of SRS are present. (A+)
The frequency of individual features in specific SRS subgroups (11p15 LOM, upd(7)mat and clinical SRS) and patients with SGA but not SRS, where data are available, are shown in Supplementary information S1 (table). Genotype–phenotype studies of patients with SRS indicate considerable overlap in clinical phenotype between (epi)genotypes, and these are generally clinically indistinguishable. However, some features are more common in particular molecular subgroups4,13,15,16,17,20,73.
Patients with 11p15 LOM tend to have a lower birth length and weight, more frequent body asymmetry and more frequent congenital anomalies than patients with upd(7)mat15,20. Neurocognitive problems are more frequent in patients with upd(7)mat than in those with 11p15 LOM or clinical SRS15,16,20 (see later section on neurocognitive problems).
Patients with 11p15 duplication encompassing H19/IGF2 IG-DMR and KCNQ1OT1 TSS-DMR have an SRS phenotype, but usually without asymmetry and with an increased likelihood of developmental delay53. Of 15 patients reported to have a 11p15 duplication encompassing H19/IGF2 IG-DMR and KCNQ1OT1 TSS-DMR, four were noted to have hearing loss74.
The differential diagnosis of children with short stature of prenatal onset includes many syndromic diagnoses and chromosomal rearrangements75 (Tables 3,4). Particular features should prompt consideration of diagnoses other than SRS. These include relative microcephaly (head circumference SDS below height and weight SDS), notable global developmental delay or intellectual disability (without a related explanation such as documented hypoglycaemia), absence of severe feeding difficulties and/or the presence of additional congenital anomalies, facial dysmorphism or other features atypical of SRS. Disproportionate short stature is suggestive of skeletal dysplasia. Photosensitive skin rash or recurrent bronchopulmonary infections should prompt investigation for chromosome breakage disorders. As SRS is generally sporadic, a family history of growth failure and/or consanguinity might suggest an alternative underlying diagnosis76. The clinical features of the most important and/or likely differential diagnoses are summarized in Tables 3,4.
A correct diagnosis can have extremely important implications for management. Response to GH treatment, if given, varies depending on the underlying syndromic diagnosis. For instance, GH treatment is contraindicated in patients with chromosome breakage disorders, such as Bloom syndrome, due to the associated risk of malignancy77. GH treatment in patients with SHORT syndrome has been reported to precipitate insulin resistance and subsequent type 2 diabetes mellitus78. An incorrect diagnosis of SRS leading to the recommendation of GH treatment could, therefore, have adverse consequences in these patients.
Three patients (one with no history of fractures) have been reported with clinical features of SRS but a molecular diagnosis of osteogenesis imperfecta, with a COL1A1 mutation79,80. Both SRS and osteogenesis imperfecta can cause prenatal onset of growth failure, relative macrocephaly, large fontanelle, blue sclerae and body asymmetry. Both diagnoses should, therefore, be considered in patients with features overlapping both conditions.
3.1 An alternative syndromic diagnosis, and specific investigation for this diagnosis, should be particularly considered in patients with any of the following: additional features atypical of SRS, family history of growth failure and/or consanguinity. (A+++)
3.2 Patients with features of SRS overlapping with osteogenesis imperfecta should have a skeletal survey to look for additional evidence for osteogenesis imperfecta, with consideration of COL1A1/2 gene testing. (A++)
SRS leads to a wide spectrum of abnormal physical characteristics and functional abnormalities. Multidisciplinary follow up and early, specific, intervention are necessary for optimum management of this group of patients.
4.1 Patients with SRS should receive multidisciplinary care in a centre of expertise in SRS in coordination with their local centre. The multidisciplinary team should be composed of paediatric subspecialists such as an endocrinologist (coordinator), gastroenterologist, dietician, clinical geneticist, craniofacial team, orthopaedic surgeon, neurologist, speech and language therapist and psychologist. (A+++)
Early feeding and nutritional support
The typical neonate with SRS has length SDS below weight SDS; but after birth, due to poor appetite, feeding difficulties and gastrointestinal problems, weight SDS drops below the length SDS4,17,73,81. Over time, progressive failure to thrive can result in a calorie-related length deficit4,15,82.
Feeding difficulties and failure to thrive are considerably more frequent in patients with SRS than in children with SGA but not SRS4,17. Failure to thrive in children with SRS is probably due to a combination of factors, including feeding difficulties (poor appetite, oromotor issues and the resulting low caloric intake) as well as functional and structural gastrointestinal problems. Digestive problems or malnutrition occur in over 70% of patients with SRS82, including severe gastrooesophageal reflux in 55%, which often results in persistent vomiting after the age of 1 year. Constipation is also common, particularly after age 2 years82. Cyproheptadine used as an appetite stimulant improves weight gain in other paediatric conditions83,84; however, specific studies of its use in SRS are needed before it can be recommended in these patients.
The main therapeutic goals for the first 2 years of life in patients with SRS are nutritional support, prevention of hypoglycaemia and recovery of any calorie-related length or height deficit, which should be addressed before initiation of GH therapy (see following sections on prevention of hypoglycaemia and GH therapy). However, careful monitoring is needed, especially during nonvolitional feeding, because rapid catch-up weight gain in children born SGA has been associated with an increased risk of metabolic and cardiovascular disease in later life85.
Children with SRS have an abnormal body composition with low muscle mass, and are typically light for their length or height3,15,86,87. From our experience, the target for healthy nutritional status is narrow, and is dependent on individual innate muscle mass and even slight overnourishment (for example, weight >90% of ideal weight for length or height) can rapidly increase relative fat mass. Suggested targets for children aged 2–4 years preparing for GH therapy are: weight 75–85% of the 50th centile weight for length or height and/or BMI 12–14 kg/m2, using height measurements on the longer side if notable leg length discrepancy is found (see following section on GH therapy). A weight below 70% of the ideal weight for length or height compromises growth velocity, despite GH treatment. For children >4 years old, the optimal target BMI will depend on their muscle mass. Two groups of patients are exceptions to this observation. Firstly, in patients with 11p15 LOM who have a very low muscle mass and considerable body asymmetry, a lower BMI might be adequate (11–12 kg/m2). Secondly, for patients with upd(7)mat with near normal muscle mass, a higher BMI might be acceptable (14–15 kg/m2).
5.1 For nutritional goals in the first years of life, we recommend nutritional repletion* with awareness of possible hazards of rapid postnatal catch-up leading to subsequent increased metabolic risk. (A+++)
5.2 Ask for and/or screen early for gut dysmotility (gastrooesophageal reflux, delayed gastric emptying and constipation) in all children. (A+++)
5.3 Diagnose and treat any oromotor and/or sensory issues that affect oral intake of food. (A+++)
5.4 In patients with severe feeding failure who are unresponsive to standard care, anatomical or functional disorders of the gastrointestinal tract, such as malrotation, should be excluded. (A+++)
5.5 Avoid enteral feeding by nasogastric or gastrostomy tube in a child capable of eating where there is adequate nutritional repletion. (A+++)
5.6 In cases of extreme feeding difficulties or gastrooesophageal reflux, consider enteral feeding by gastrostomy tube (with or without fundoplication) or low-profile transgastric jejunostomy as a last resort to protect against hypoglycaemia and/or malnutrition. (A+++)
5.7 In the case of enteral feeding, prevent excessive weight gain in both volitionally and nonvolitionally fed children. (A++)
*Low muscle mass makes typical BMI targets excessive in this population. Targets currently used in some centres include: Waterlow score 75–85% (Ref. 88); weight-for-length SDS −2 to −1 in first year of life; BMI target SDS between −2 to −1 after first year of life.
Prevention of hypoglycaemia
Young children with SRS, particularly under age 5 years, have low muscle and liver mass, a disproportionately large brain-for-body size and feeding difficulties, all of which increase their risk of fasting hypoglycaemia and its potential neurocognitive consequences. The incidence of hypoglycaemia in these children is approximately 27%20, with a high frequency of spontaneous, asymptomatic nocturnal hypoglycaemia89.
Monitoring of levels of urinary ketones is usually effective in pre-empting hypoglycaemia related to fasting, activity or illness. This measurement can be used to determine the 'safe fasting time' for a child, which will change with age. Night time hypoglycaemia can be prevented by adding either high molecular weight glucose polymer (for infants under 10 months) or uncooked corn starch (for older infants and children particularly at risk) to the last evening feed. Dental hygiene is important as complex carbohydrates can promote cavities90. Severe, non-fasting and non-ketotic hypoglycaemia should always be identified and investigated further.
For episodes of preoperative fasting or febrile illness, intravenous glucose (10% dextrose) might be required. Children with SRS might need longer periods of gut rest than children with SGA but not SRS before oral or enteral feeding because of their gut dysmotility and intrinsic feeding defects. Before discharge, it is advisable to achieve an absence of ketonuria following at least 12 h of feeding, without intravenous support. When hypoglycaemia remains a problem, early GH therapy should be considered91,92 (see following section on GH therapy).
6.1 Monitoring for ketonuria at home is useful to determine which children need intervention for impending hypoglycaemia. (A++)*
6.2 Develop a plan with the child's local paediatrician and emergency room for rapid admission and intravenous dextrose treatment when the child is ill. (A++)
6.3 Admit children with SRS to hospital early in the course of an illness associated with ketonuria or hypoglycaemia and do not discharge them until they are metabolically stable and can be adequately fed. (A++)
6.4 Glucagon is not recommended to correct hypoglycaemia, because of poor glycogen stores and limited ability for gluconeogenesis. (A+++)
6.5 Provide parents with an emergency guidance plan for illnesses. (A+++)
6.6 Teach parents how to recognize signs of hypoglycaemia, measure ketones, determine the 'safe fasting time' for their child, prevent hypoglycaemia using complex carbohydrates and avoid fasting outside a controlled environment. (A+++)
6.7 In severe cases of fasting hypoglycaemia, where other causes have been excluded and if other alternatives are ineffective, consider:
Early start of GH therapy to support glucose sources (increase in muscle mass and gluconeogenesis) (A++)
Placement of a gastrostomy tube or jejunostomy tube. (A++)
*Children with a history of hypoglycaemia who do not have an appropriate ketone response will require formal fasting studies.
Surgery and anaesthesia
Any surgery should be carefully planned due to the increased risk of fasting hypoglycaemia in patients with SRS93. As a result of their diminished weight-for-height ratio, low BMI and large head, young patients with SRS are at risk of hypothermia in a cool operating room94. Many children with SRS also have abnormal tooth distribution and a small mandible, which affects airway visualization and intubation95. Finally, young children with SRS who are malnourished might not heal well following surgery96.
7.1 Review issues related to SRS with the anaesthetist and surgeon in advance. (A+++)
7.2 Consider admission the night before surgery for early administration of intravenous dextrose before surgery to avoid ketonuria and hypoglycaemia. (A++)
7.3 Schedule first on the surgical list where possible. (A++)
7.4 Monitor blood glucose and administer intravenous dextrose during and after surgery. Do not discharge until ketonuria is absent and the child can sustain themselves on oral or enteral feeding. (A++)
7.5 Follow the intraoperative temperature maintenance protocol appropriate for the patient's size, not age. (A+++)
7.6 Delay elective surgery until the child is adequately nourished. (B+)
7.7 Be aware of the high risk of malnutrition after surgery and follow appropriate guidelines. (A+)
Growth hormone treatment
Data on adult height in untreated patients with SRS are limited; however, SRS is associated with a significant reduction in adult height (around −3 SDS; Supplementary information S4 (table)) (Ref. 3). SRS is an indication for growth-promoting GH treatment under the SGA registered licence. It is worth noting that SRS was the only syndrome to be included in the clinical trials of GH in short children born SGA that led to the US FDA and the European Medicines Agency (EMA) SGA indications for GH therapy in 2001 and 2003, respectively97,98,99,100,101. The results of these clinical trials, therefore, validate the use of GH for patients with SRS.
Overall, clinical trials of GH treatment in patients with SGA (in which patients with SRS were included) demonstrated a satisfactory growth response and an increase in predicted adult height of 7–11 cm at pharmacological doses of GH97,98,99,100,102. However, the response in patients with SRS was not investigated until a Dutch longitudinal study analysed the response to GH in 62 children with a clinical diagnosis of SRS using the NH-CSS compared with 227 short, non-syndromic children born SGA. Overall, the study showed a similar response to GH in patients with SRS compared with non-SRS children born SGA (mean total height gains of 1.30 SDS and 1.26 SDS, respectively); however, the final adult height attained in patients with SRS was lower (mean adult height −2.17 SDS versus −1.65 SDS for non-SRS children born SGA)87. Although the mean height at the start of GH treatment in patients with SRS was statistically significantly lower than in those without SRS, it was shown that patients with all SRS subtypes benefited from GH treatment, with a trend towards increased height gain in patients with upd(7)mat or clinical SRS. In addition, some interim100,102 and long-term103,104 studies have focused on the response to GH specifically in patients with SRS, albeit without a control group of non-SRS short children born SGA. Strong predictors of the short-term and long-term responses to GH were age and height SDS at the start of GH treatment (both inversely related)103,104,105. However, the study by Rakover et al.105 of 33 patients with SRS lacked data on adult height. Mean total height gain ranged from +1.2 to +1.4 SDS for GH doses of 35–70 µg/kg per day, which is similar to that achieved in patients with non-syndromic SGA97,103,104. In 2007, an SGA consensus statement advocated early treatment with GH for children born SGA, including those with SRS, who had severe growth retardation (height SDS ≤2.5; age 2–4 years; dose 35–70 µg/kg per day)106.
Additional potential benefits of GH treatment are increases in appetite, lean body mass and muscle power, which can result in improved mobility86,107. In patients with Prader–Willi syndrome, another imprinting disorder, GH treatment started in infancy results in increased lean body mass and motor development, as well as decreased fat mass108,109; consequently, GH treatment is now recommended from infancy in this condition. Children with SRS who are <2 years old typically present with low muscle mass and hypotonia, similarly to patients with Prader–Willi syndrome15, and could also benefit from early GH treatment. Further studies are necessary to investigate this option in patients with SRS.
Classic GH deficiency is neither a common nor a relevant cause of short stature in SRS, nor is it predictive of the response to GH treatment in children born SGA103,105,110. Furthermore, given the risk of hypoglycaemia associated with fasting required for GH testing, testing children with SRS might carry added risks.
For most children with SRS, an increase in height velocity of ≥3 cm per year is the lower limit of an effective response range106. The growth response depends on the patient's age, GH dose, height deficit, rate of weight gain and confounding problems such as intercurrent illness and scoliosis.
Levels of insulin-like growth factor 1 (IGF1) in response to GH treatment in patients with SRS are difficult to interpret. Children with 11p15 LOM have significantly higher IGF1 levels than children with upd(7)mat and other children born SGA, which suggests an element of IGF1 resistance in patients with 11p15 LOM73,111. Basal serum levels of IGF1 in the upper quartile of the normal age-related range or higher can be expected in children with SRS, especially those with 11p15 LOM73. In children with 11p15 LOM, serum levels of insulin-like growth factor-binding protein 3 (IGFBP3) are also elevated111. IGF1 levels might rise significantly above the reference range in children with SRS on standard doses of GH87,111. Further studies are needed to understand how best to use IGF1 and IGFBP3 serum levels to monitor GH doses in children with SRS and IGF1 resistance.
Comprehensive reviews on the use of GH in children born SGA have concluded that GH treatment seems to be safe and effective112. Adverse effects due to GH treatment are no more frequent in children with SRS than in those with non-syndromic SGA87,113 and no specific precautions are advised.
8.1 Defer GH treatment until caloric deficits are addressed. (A++)
8.2 Avoid GH stimulation testing. (A++)
8.3 Goals of GH treatment are to improve body composition (especially lean body mass), psychomotor development and appetite, to reduce the risk of hypoglycaemia, and to optimise linear growth. (A++)
8.4 Treat with GH as soon as possible; starting at age 2–4 years is adequate for the majority of patients; however, due consideration should be given to the exceptions listed below*. (A++)
8.5 Start GH at a dose of approximately 35 µg/kg per day. Use the lowest dose that results in catch-up growth. (A+++)
8.6 Terminate GH therapy when height velocity is <2 cm per year over a 6-month period and bone age is >14 years (female patients) or >17 years (male patients). (A++)
8.7 If response to GH is poor, re-evaluate the underlying diagnosis, GH dose, IGF1 response, adherence to therapy and other confounding systemic problems. (A+++)
8.8 Monitor circulating levels of IGF1 and IGFBP3 at least yearly during GH treatment. (A++)
*GH treatment does not have a specific indication for SRS and is prescribed under the SGA indication (height SDS −2.5; age >2–4 years; dose 35–70 µg/kg per day)106. Exemptions from the current SGA licensed indication used in some centres include starting GH therapy below the age of 2 years in case of: severe fasting hypoglycaemia; severe malnutrition, despite nutritional support, which will lead to gastrostomy if no improvement is seen; and severe muscular hypotonia.
Bone age advancement and puberty
The published literature on the natural history of bone age progression in patients with SRS is limited. Early bone age delay is followed by rapid advancement typically at around 8–9 years of age3,81,113 but sometimes much younger, especially in nonvolitionally overfed children. Onset of puberty is usually within the normal range (8–13 years in girls and 9–14 years in boys)114 but at the younger end of the spectrum3,73,87,115. Adrenarche can be early and aggressive in comparison with children born with non-SRS SGA, particularly in those with 11p15 LOM116.
Our experience is that in patients with SRS and early adrenarche, the onset of central puberty might be earlier and the tempo faster than expected. In the past few decades, population studies analysing the timing of normal puberty observed a mean age of puberty onset of 9.7–10.0 years in girls114. As a group, girls with SRS seem to start central puberty at a mean age of 9.1 years (I. Netchine, unpublished work). This early puberty further accelerates bone age maturation, which leads to an attenuated pubertal growth spurt and compromised adult height. Children with upd(7)mat are likely to progress to central puberty at an even younger age than patients with SRS and 11p15 LOM (mean starting age 8.5 years in girls and 9.5 years in boys) (I. Netchine, unpublished work). A rapid increase in BMI might also exacerbate the tendency to early adrenarche and central puberty117,118,119.
The window for effective GH treatment seems to be shorter in patients with SRS than in non-SRS patients with SGA. In a study comparing a cohort of patients with SRS and a cohort of patients born SGA but without SRS, puberty started significantly earlier in the former (at 10.2 years versus 11.2 years in girls with SRS and non-SRS SGA, respectively, and at 11.4 years versus 12.0 years in boys with SRS and non-SRS SGA, respectively)87. Furthermore, a steeper decline in height SDS from the onset of puberty until adult height was seen in patients with SRS, which contributed to a lower adult height and a larger distance to target height than in non-SRS patients with SGA. However, in 17 patients with SRS in this study, puberty was postponed for 2 years with gonadotropin-releasing hormone analogue (GnRHa) due to a low predicted adult height. The effect of GnRHa on final height has been analysed in a cohort of patients with SGA, including patients with SRS120,121. This analysis suggested that the combination of GnRHa, started at the initiation of puberty and continued for at least 2 years, along with GH treatment, improves adult height in patients born SGA with a poor adult height prognosis. A retrospective study of GnRHa treatment specifically in patients with SRS did not detect an effect of GnRHa on adult height, but this therapy was used in only 16 of 37 patients and was not standardized104. Further studies are required to specifically look at its effects in patients with SRS.
Aromatase catalyses the rate-limiting step in the conversion of androstenedione to oestrone and testosterone to oestradiol. In patients with adrenarche with advancing bone age, but without central puberty, third-generation aromatase inhibitors (such as anastrozole) might be helpful in preventing rapid bone maturation, but are currently not licensed for growth disorders122. An 18-month double-blind clinical trial is currently underway to study the efficacy and tolerance of treatment with anastrozole to slow bone maturation related to pathological adrenarche in patients with SRS and Prader–Willi syndrome123.
9.1 Monitor for signs of premature adrenarche, fairly early and accelerated central puberty, and insulin resistance. (A+++)
9.2 Monitor and anticipate acceleration of bone age especially from mid childhood. (A++)
9.3 Consider personalized treatment with GnRHa for at least 2 years in children with evidence of central puberty (starting no later than age 12 years in girls and age 13 years in boys) to preserve adult height potential. (A++)
Long-term metabolic complications
Individuals born with a low birth weight are at increased risk of adult health problems including coronary heart disease124,125,126, hypertension, dyslipidaemia, insulin resistance and obesity (the metabolic syndrome)127,128,129,130. Studies of children born SGA indicate that those who have rapid or disproportionate catch-up in weight are at particularly high risk119,131,132.
Insulin resistance in young, pre-pubertal, children with SRS can be atypical and difficult to detect in the fasting state; however, impaired glucose tolerance can be confirmed on formal oral glucose tolerance testing133,134. Insulin resistance becomes more classic in the pubertal or post-pubertal age groups with elevation in fasting levels of glucose and insulin, and possibly the development of type 2 diabetes mellitus135,136.
Overall, GH therapy seems to have positive metabolic effects in children born SGA137, but specific data on such effects in SRS are lacking. Many studies of long-term GH treatment in children born SGA have shown positive outcomes, including increased lean body mass, reduced fat mass, decreased blood pressure and an improved lipid profile107,120,137,138, which might last after discontinuation of therapy138,139.
In a study of 110 children born SGA treated with GH, those with the highest baseline levels of IGF1 were the least insulin sensitive. Gains in height and IGF1 response were positively associated with insulin secretion140. In SRS, children with 11p15 LOM seem to be at a higher metabolic risk than children who have upd(7)mat and other children born SGA due to poor muscle mass and raised levels of IGF1 (Refs 15,16,73,87). Further research is, therefore, required on the long-term effects of GH therapy on body composition and metabolic parameters in SRS and its various genotypes.
10.1 Avoid excessive or rapid weight gain to prevent increased insulin resistance, which is associated with early and rapidly advancing adrenarche, early central puberty, and, in girls, a future risk of developing polycystic ovary syndrome. (A++)
10.2 Raise awareness among gastroenterologists, dieticians, neonatologists, paediatricians and primary health-care providers of the importance of not overfeeding this group of children. (A+++)
10.3 Advise parents, grandparents and care-givers about the risk of insulin resistance associated with intrauterine growth retardation and overfeeding. (A+++)
10.4 Screen for physical and biochemical indicators of insulin resistance during GH treatment, especially in children with low muscle mass and high baseline levels of IGF1. (A+)
10.5 In patients with clinical signs of insulin resistance, consider formal assessment of insulin sensitivity with a 2-h oral glucose tolerance test including measurement of insulin and C-peptide levels (A++)
10.6 Advocate a healthy diet and lifestyle in older children and young adults with particular emphasis on protein calorie balance and regular exercise to avoid disproportionate weight gain, particularly after discontinuation of GH treatment. (A+++)
Motor and speech delay are common in children with SRS4,16,17,18,20 (Table 2). Motor delay might be related to reduced muscle bulk and fairly large head size. Verbal dyspraxia and more global developmental delay or learning difficulties, usually mild, have been described in some children with SRS, particularly those with upd(7)mat12,15,16,20,141. Autistic spectrum disorder has also been reported more frequently in this subgroup than in the other subgroups of SRS15. Myoclonus dystonia in patients with upd(7)mat is probably associated with altered expression of the paternally expressed SGCE on chromosome 7q21 (Refs 20,40,142,143).
11.1 Refer infants and children with SRS for a developmental assessment when necessary to ensure appropriate intervention as early as possible. (A+++)
11.2 In patients with upd(7)mat, check for symptoms of myoclonus dystonia at each clinical appointment and refer early to a paediatric neurologist if required. (A+++)
11.3 Monitor children with upd(7)mat for signs of verbal or oromotor dyspraxia and/or signs of autistic spectrum disorders. (A+++)
11.4 Inform parents about increased risk of speech, oromotor and learning disabilities (especially in those with upd(7)mat). (A+++)
11.5 Follow up school-age children for any learning difficulties, psychosocial challenges and/or cognitive delay, to enable appropriate intervention. (A+++)
Orthopaedic problems seen in association with SRS include limb or body asymmetry, scoliosis, hip dysplasia and hand and/or foot anomalies (Table 2).
Limb asymmetry can affect the arms, legs or both. In seven patients with clinically diagnosed SRS, limb length discrepancy was not significantly affected by GH treatment144. Limb lengthening surgery performed to equalize limb lengths in patients with SRS has shown positive results145.
Scoliosis has been reported in 9–36% of individuals with SRS20,146,147. The causal relationship to leg length asymmetry is not clear146,147. Associated back pain has been reported inconsistently5,146. GH therapy might be associated with worsening of existing scoliosis; however, causality has not been established148. A study in a large group of children with Prader–Willi syndrome (an imprinting disorder with clinical features that overlap with those of SRS: growth failure; infant hypotonia; early feeding difficulties; and an increased risk of scoliosis) has clearly shown that GH therapy does not influence onset and progression of scoliosis149; however, specific studies are required to determine whether GH therapy modifies the risk of scoliosis in patients with SRS.
12.1 Where necessary, refer to a paediatric orthopaedic surgeon for collaborative management of body asymmetry, limb length discrepancy and scoliosis. (A+++)
12.2 Routinely examine all patients with SRS for scoliosis. (A+++)
12.3 Before initiation of GH therapy, refer patients with scoliosis to the orthopaedic team and monitor while receiving GH. (A+++)
12.4 Evaluate leg length asymmetry regularly and consider orthopaedic management if necessary. (A++)
SRS is characterized by craniofacial disproportion, which results in a triangular-shaped face95. Delayed dental eruption, microdontia, absence of secondary teeth and blunted condyles have all been reported in patients with SRS150,151,152.
In our experience, the upper jaw arch is frequently narrow and crowded, but crowding might be severe in the lower arch, with displacement of lower incisors into a lingual position. Micrognathia is frequent, with lack of mandibular growth, which results in a small, pointed chin and an overbite. Children with notable facial asymmetry might have a crossbite that impairs normal chewing. Velopharyngeal insufficiency with or without a submucous cleft is quite common in patients with 11p15 LOM SRS20. Otitis media is frequent in young children with SRS7 and seems to be improved by orthodontic treatment20.
Orthodontic intervention in children with SRS can help normalize oropharangeal function and facial appearance. An experienced craniofacial team, including orthodontists, plastic surgeons and ear, nose and throat surgeons is ideal. Multiple orthodontic techniques have been used successfully153. Currently, rapid palatal expansion is the most effective technique to change the shape of the face154.
Many patients with SRS report excessive daytime fatigue, snoring and/or disrupted sleep. However, data are very limited regarding sleep problems, including sleep disordered breathing, in association with SRS. A retrospective study identified mild sleep disordered breathing in 74% of patients with SRS (not exacerbated with GH therapy)155. Further studies are necessary.
13.1 Develop a referral relationship with a maxillofacial team or orthodontist who has experience caring for patients with SRS. (A++)
13.2 Refer patients to the maxillofacial team for assessment after eruption of primary dentition when necessary. (A++)
13.3 Encourage early orthodontic intervention and compliance with follow-up. (A+)
13.4 Screen for symptoms of sleep disordered breathing (such as snoring, apnoeas, excessive daytime fatigue, disrupted sleep and agitation). (A++)
13.5 Refer patients with suspected sleep disordered breathing to the appropriate specialist for evaluation of obstructive sleep apnoea. (A++)
Other congenital anomalies
Congenital anomalies have been described in a minority of patients with SRS, particularly those with 11p15 LOM (see Supplementary information S1 (table)). Genital abnormalities, including cryptorchidism and hypospadias, occur frequently in boys16,20. Mayer–Rokitansky–Kuster–Hauser syndrome in female patients is characterized by congenital hypoplasia or aplasia of the uterus and upper part of the vagina16,18,156,157. Structural renal anomalies18,20 and congenital heart defects4,18,20,158 have also been reported.
14.1 Investigate genital abnormalities in boys. (A+++)
14.2 Investigate girls with primary amenorrhoea for Mayer–Rokitansky–Kuster–Hauser syndrome. (A+++)
Very little information exists in the literature regarding the long-term natural history of SRS. The majority of individuals with SRS are not routinely followed up, and the small numbers of adults reported have few medical problems. However, it is well recognized that being SGA at birth with accelerated gain in weight for length, particularly during early life, increases the risk of metabolic problems in adulthood119,132,159 (see previous discussion). Medical problems reported in adult patients with 11p15 LOM include hypertension, dilated cardiomyopathy, type 2 diabetes mellitus, hypercholesterolaemia, fatty liver infiltration, elevated glucose levels and raised HbA1c levels135,136,160; however, these reports might not be representative of the population as a whole.
15.1 Consider medical follow-up of adolescents and young adult patients with SRS or develop collaboration with a general or internal medicine team for follow-up. (A+++)
15.2 Avoid losing contact with adult patients with SRS, to facilitate their participation in, and potential benefit from, future clinical research. (A+++)
Accurate genetic counselling depends on the underlying molecular cause. 11p15 LOM is associated with a low recurrence risk (with parents of a child with SRS being unlikely to have another affected child). The offspring risk is also low (meaning that individuals with SRS are unlikely to pass the condition on to their children). However, empirical figures are not available. Only three sibships with 11p15 LOM are reported in the literature13,20, and the underlying mechanism is unknown in all three.
The potential for a familial trans-acting gene mutation suggests that the recurrence risk in patients with SRS and MLID could be higher than in other patients with SRS; however, evidence to support this supposition does not yet exist.
Rare familial cases of SRS have been reported with underlying mechanisms including: maternally inherited 11p15 duplication24,26 (see Supplementary information S2 (table)); maternally inherited CDKN1C gain-of-function mutations60; and paternally inherited IGF2 loss-of-function mutations61. In these families, the risk of recurrence might be as high as 50%24,26,60,61. Investigation for underlying CNVs in patients with 11p15 LOM is, therefore, important. upd(7)mat is associated with a low recurrence and offspring risk (if the karyotype of the patient is normal)50. Data are limited regarding the risk of parents of children with clinically diagnosed SRS having another child with SRS; however, the overall risk is probably low. Similarly, the offspring risk for individuals with clinically diagnosed SRS is likely to be low.
16.1 Genetic counselling should be performed by a health professional experienced in the field of imprinting disorders. As the recurrence risk associated with CNVs is dependent on their size, location and parental origin, these should be taken into consideration during counselling for the family. (A+++)
Children with SRS and their families face challenges from birth to adulthood. In addition to the problems associated with being born SGA, clinicians treating patients with SRS need to be aware of syndrome-specific management issues. These include substantial feeding difficulties, severe postnatal growth failure with no catch-up, recurrent hypoglycaemia, premature adrenarche, fairly early and rapid puberty, insulin resistance, body asymmetry, orthodontic issues, sleep disordered breathing and the potential for other congenital anomalies.
Presented here are the first international consensus guidelines for the diagnosis and management of SRS, based on published evidence and expert opinion. A summary of all 72 recommendations, including a flow chart for the investigation and diagnosis of SRS, is available as supplementary information online (see Supplementary information S5).
These management recommendations apply to all patients clinically diagnosed with SRS, both with and without a molecularly confirmed diagnosis. However, identification of the underlying molecular subtype can guide treatment with regard to specific risk factors. Management should involve a multi-disciplinary approach and close parental guidance. A practical checklist for use in routine clinical follow up of these patients is proposed in Table 5.
As published data specific to SRS are limited, many questions remain (Box 2). International collaboration and further research is urgently needed to better inform the investigation and management of patients with SRS in the future.
Silver, H. K., Kiyasu, W., George, J. & Dearner, W. C. Syndrome of congenital hemihypertrophy, shortening of stature and elevated urinary gonadotropins. Pediatrics 12, 368–373 (1953).
Russell, A. A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples). Proc. R. Soc. Med. 47, 1040–1044 (1954).
Wollmann, H. A., Kirchner, T., Enders, H., Preece, M. A. & Ranke, M. B. Growth and symptoms in Silver–Russell syndrome: review on the basis of 386 patients. Eur. J. Pediatr. 154, 958–968 (1995).
Netchine, I. et al. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell–Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations. J. Clin. Endocrinol. Metab. 92, 3148–3154 (2007).
Price, S. M., Stanhope, R., Garrett, C., Preece, M. A. & Trembath, R. C. The spectrum of Silver–Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J. Med. Genet. 36, 837–842 (1999).
Wakeling, E. L. Silver–Russell syndrome. Arch. Dis. Child 96, 1156–1161 (2011).
Toutain, A. Silver–Russell syndrome. Orphanet http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=584&Disease_Disease_Search_diseaseGroup=Silver-Russell-syndrome&Disease_Disease_Search_diseaseType=Pat&Disease(s)/group%20of%20diseases=Silver-Russell-syndrome&title=Silver-Russell-syndrome&search=Disease_Search_Simple (2007).
Yakoreva, M. et al. A retrospective analysis of the prevalence of imprinting disorders in Estonia. Eur. J. Hum. Genet. 23 (Suppl. 1), 325 (2015).
Gicquel, C. et al. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver–Russell syndrome. Nat. Genet. 37, 1003–1007 (2005).
Schönherr, N. et al. (Epi)mutations in 11p15 significantly contribute to Silver–Russell syndrome: but are they generally involved in growth retardation? Eur. J. Med. Genet. 49, 414–418 (2006).
de Villiers, M. R., de Villiers, P. J. & Kent, A. P. The Delphi technique in health sciences education research. Med. Teach 27, 639–643 (2005).
Lai, K. Y., Skuse, D., Stanhope, R. & Hindmarsh, P. Cognitive abilities associated with the Silver–Russell syndrome. Arch. Dis. Child 71, 490–496 (1994).
Bartholdi, D. et al. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver–Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. J. Med. Genet. 46, 192–197 (2009).
Dias, R. P. et al. Comparison of the clinical scoring systems in Silver–Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing. J. Med. Genet. 50, 635–639 (2013).
Azzi, S. et al. A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver–Russell syndrome. J. Med. Genet. 52, 446–453 (2015).
Bruce, S., Hannula-Jouppi, K., Peltonen, J., Kere, J. & Lipsanen-Nyman, M. Clinically distinct epigenetic subgroups in Silver–Russell syndrome: the degree of H19 hypomethylation associates with phenotype severity and genital and skeletal anomalies. J. Clin. Endocrinol. Metab. 94, 579–587 (2009).
Fuke, T. et al. Molecular and clinical studies in 138 Japanese patients with Silver–Russell syndrome. PLoS ONE 8, e60105 (2013).
Bliek, J. et al. Hypomethylation of the H19 gene causes not only Silver–Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype. Am. J. Hum. Genet. 78, 604–614 (2006).
Eggermann, T. et al. Broad clinical spectrum in Silver–Russell syndrome and consequences for genetic testing in growth retardation. Pediatrics 123, e929–e931 (2009).
Wakeling, E. L. et al. Epigenotype–phenotype correlations in Silver–Russell syndrome. J. Med. Genet. 47, 760–768 (2010).
Russo, S. et al. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes. Clin. Epigenetics 8, 23 (2016).
Hannula, K. et al. Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause. Pediatrics 109, 441–448 (2002).
Zeschnigk, M. et al. IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia. Eur. J. Hum. Genet. 16, 328–334 (2008).
Demars, J. & Gicquel, C. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith–Wiedemann and Silver–Russell syndromes. Clin. Genet. 81, 350–361 (2012).
Eggermann, T., Spengler, S., Gogiel, M., Begemann, M. & Elbracht, M. Epigenetic and genetic diagnosis of Silver–Russell syndrome. Expert Rev. Mol. Diagn. 12, 459–471 (2012).
Begemann, M. et al. Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature. J. Med. Genet. 49, 547–553 (2012).
Eggermann, K. et al. EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome. Eur. J. Hum. Genet. http://dx.doi.org/10.1038/ejhg.2016.45 (2016).
Alders, M., Bliek, J., vd Lip, K., vd Bogaard, R. & Mannens, M. Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis. Eur. J. Hum. Genet. 17, 467–473 (2009).
Azzi, S. et al. Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes. Hum. Mutat. 32, 249–258 (2011).
Begemann, M. et al. Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci. Epigenetics 7, 473–481 (2012).
Eggermann, T. et al. Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver–Russell syndrome. Clin. Genet. 73, 79–84 (2008).
Scott, R. H. et al. Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation. J. Med. Genet. 45, 106–113 (2008).
Azzi, S. et al. Complex tissue-specific epigenotypes in Russell–Silver syndrome associated with 11p15 ICR1 hypomethylation. Hum. Mutat. 35, 1211–1220 (2014).
Begemann, M. et al. Silver–Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. Clin. Genet. 80, 83–88 (2011).
Kotzot, D. et al. Uniparental disomy 7 in Silver–Russell syndrome and primordial growth retardation. Hum. Mol. Genet. 4, 583–587 (1995).
Preece, M. A. et al. Maternal uniparental disomy 7 in Silver–Russell syndrome. J. Med. Genet. 34, 6–9 (1997).
Preece, M. A. et al. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver–Russell syndrome probands. J. Med. Genet. 36, 457–460 (1999).
Spence, J. E. et al. Uniparental disomy as a mechanism for human genetic disease. Am. J. Hum. Genet. 42, 217–226 (1988).
Voss, R. et al. Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans? Am. J. Hum. Genet. 45, 373–380 (1989).
Bulli, C. et al. Recessive congenital myotonia resulting from maternal isodisomy of chromosome 7: a case report. Cases J. 2, 7111 (2009).
Monk, D. et al. Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. Hum. Genet. 111, 376–387 (2002).
Joyce, C. A., Sharp, A., Walker, J. M., Bullman, H. & Temple, I. K. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver–Russell syndrome. Hum. Genet. 105, 273–280 (1999).
Monk, D. et al. Duplication of 7p11.2-p13, including GRB10, in Silver–Russell syndrome. Am. J. Hum. Genet. 66, 36–46 (2000).
Hannula, K., Lipsanen-Nyman, M., Kontiokari, T. & Kere, J. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver–Russell syndrome delimits a candidate gene region. Am. J. Hum. Genet. 68, 247–253 (2001).
Reboul, M. P. et al. Mosaic maternal uniparental isodisomy for chromosome 7q21-qter. Clin. Genet. 70, 207–213 (2006).
Leach, N. T., Chudoba, I., Stewart, T. V., Holmes, L. B. & Weremowicz, S. Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndrome. Am. J. Med. Genet. A143A, 1489–1493 (2007).
Eggermann, T. et al. Segmental maternal UPD(7q) in Silver–Russell syndrome. Clin. Genet. 74, 486–489 (2008).
Eggermann, T. et al. Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver–Russell syndrome features. Clin. Genet. 81, 298–300 (2012).
Hattori, M. et al. Diagnosis of Russell–Silver syndrome by the combined bisulfite restriction analysis-denaturing high-performance liquid chromatography assay. Genet. Test. Mol. Biomarkers 13, 623–630 (2009).
Hoffmann, K. & Heller, R. Uniparental disomies 7 and 14. Best Pract. Res. Clin. Endocrinol. Metab. 25, 77–100 (2011).
Canton, A. P. et al. Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways. Eur. J. Endocrinol. 171, 253–262 (2014).
Bruce, S. et al. Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients. J. Med. Genet. 47, 816–822 (2010).
Fokstuen, S. & Kotzot, D. Chromosomal rearrangements in patients with clinical features of Silver–Russell syndrome. Am. J. Med. Genet. A164A, 1595–1605 (2014).
Keren, B. et al. SNP arrays in Beckwith–Wiedemann syndrome: an improved diagnostic strategy. Eur. J. Med. Genet. 56, 546–550 (2013).
Ioannides, Y., Lokulo-Sodipe, K., Mackay, D. J., Davies, J. H. & Temple, I. K. Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases. J. Med. Genet. 51, 495–501 (2014).
Kagami, M. et al. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver–Russell syndrome-compatible phenotype. Eur. J. Hum. Genet. 23, 1062–1067 (2015).
Poole, R. L. et al. Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders. Am. J. Med. Genet. A161A, 2174–2182 (2013).
Eggermann, T. et al. Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients. J. Med. Genet. 38, 86–89 (2001).
Mulchandani, S. et al. Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure. Genet. Med. 18, 309–315 (2016).
Brioude, F. et al. CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome. J. Med. Genet. 50, 823–830 (2013).
Begemann, M. et al. Paternally inherited IGF2 mutation and growth restriction. N. Engl. J. Med. 373, 349–356 (2015).
Obermann, C. et al. Searching for genomic variants in IGF2 and CDKN1C in Silver–Russell syndrome patients. Mol. Genet. Metab. 82, 246–250 (2004).
Muller, A., Soellner, L., Binder, G., Begemann, M. & Eggermann, T. No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders. Am. J. Med. Genet. A170A, 283–284 (2016).
Azzi, S. et al. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum. Mol. Genet. 18, 4724–4733 (2009).
Turner, C. L. S. et al. Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. Eur. J. Hum. Genet. 18, 648–655 (2010).
Eggermann, T. et al. Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing. J. Mol. Med. (Berl.) 92, 769–777 (2014).
Court, F. et al. Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes. Hum. Mutat. 34, 595–602 (2013).
Prickett, A. R. et al. Genome-wide methylation analysis in Silver–Russell syndrome patients. Hum. Genet. 134, 317–332 (2015).
Docherty, L. E. et al. Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes. J. Med. Genet. 51, 229–238 (2014).
Rezwan, F. I. et al. A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders. Clin. Epigenetics 7, 48 (2015).
Docherty, L. E. et al. Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans. Nat. Commun. 6, 8086 (2015).
Court, F. et al. Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment. Genome Res. 24, 554–569 (2014).
Binder, G. et al. The endocrine phenotype in Silver–Russell syndrome is defined by the underlying epigenetic alteration. J. Clin. Endocrinol. Metab. 93, 1402–1407 (2008).
Nakashima, S. et al. Silver–Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C. J. Hum. Genet. 60, 91–95 (2015).
Hall, J. G. Review and hypothesis: syndromes with severe intrauterine growth restriction and very short stature—are they related to the epigenetic mechanism(s) of fetal survival involved in the developmental origins of adult health and disease? Am. J. Med. Genet. A152A, 512–527 (2010).
Akawi, N. A., Ali, B. R., Hamamy, H., Al-Hadidy, A. & Al-Gazali, L. Is autosomal recessive Silver–Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum? Am. J. Med. Genet. A155A, 1236–1245 (2011).
Renes, J. S., Willemsen, R. H., Wagner, A., Finken, M. J. & Hokken-Koelega, A. C. Bloom syndrome in short children born small for gestational age: a challenging diagnosis. J. Clin. Endocrinol. Metab. 98, 3932–3938 (2013).
Verge, C. F., Donaghue, K. C., Williams, P. F., Cowell, C. T. & Silink, M. Insulin-resistant diabetes during growth hormone therapy in a child with SHORT syndrome. Acta Paediatr. 83, 786–788 (1994).
Parker, M. J. et al. Type 1 collagenopathy presenting with a Russell–Silver phenotype. Am. J. Med. Genet. A155A, 1414–1418 (2011).
Cianci, P. et al. Collagenopathy with a phenotype resembling silver–russell syndrome phenotype. Am. J. Med. Genet. A161A, 2681–2684 (2013).
Vu-Hong, T. A. et al. Russell–Silver syndrome with 11p15 epimutation: analysis of growth, bone maturation, puberty and response to GH treatment on a large series of 101 patients. Horm. Res. 72, 447–448 (2009).
Marsaud, C., Rossignol, S., Tounian, P., Netchine, I. & Dubern, B. Prevalence and management of gastrointestinal manifestations in Silver–Russell syndrome. Arch. Dis. Child 100, 353–358 (2015).
Epifanio, M. et al. A randomized, double-blind, placebo-controlled trial of cyproheptadine for appetite stimulation in cystic fibrosis. J. Pediatr. (Rio J.) 88, 155–160 (2012).
Chinuck, R., Dewar, J., Baldwin, D. R. & Hendron, E. Appetite stimulants for people with cystic fibrosis. Cochrane Database Syst. Rev. 7, CD008190 (2014).
Ezzahir, N. et al. Time course of catch-up in adiposity influences adult anthropometry in individuals who were born small for gestational age. Pediatr. Res. 58, 243–247 (2005).
Schweizer, R., Martin, D. D., Schonau, E. & Ranke, M. B. Muscle function improves during growth hormone therapy in short children born small for gestational age: results of a peripheral quantitative computed tomography study on body composition. J. Clin. Endocrinol. Metab. 93, 2978–2983 (2008).
Smeets, C. C., Zandwijken, G. R., Renes, J. S. & Hokken-Koelega, A. C. Long-term results of GH treatment in Silver–Russell syndrome (SRS): do they benefit the same as non-SRS short-SGA? J. Clin. Endocrinol. Metab. 101, 2105–2112 (2016).
Waterlow, J. C. Classification and definition of protein-calorie malnutrition. BMJ 3, 566–569 (1972).
Azcona, C. & Stanhope, R. Hypoglycaemia and Russell–Silver syndrome. J. Pediatr. Endocrinol. Metab. 18, 663–670 (2005).
O'Connell, A. C., O'Connell, S. M., O'Mullane, E. & Hoey, H. M. Oral health of children born small for gestational age. Ir. Med. J. 103, 275–278 (2010).
Blissett, J., Harris, G. & Kirk, J. Effect of growth hormone therapy on feeding problems and food intake in children with growth disorders. Acta Paediatr. 89, 644–649 (2000).
Boonstra, V. H. et al. Food intake of children with short stature born small for gestational age before and during a randomized GH trial. Horm. Res. 65, 23–30 (2006).
Tomiyama, H., Ibuki, T., Nakajima, Y. & Tanaka, Y. Late intraoperative hypoglycemia in a patient with Russell–Silver syndrome. J. Clin. Anesth. 11, 80–82 (1999).
Scarlett, M. D. & Tha, M. W. Russell–Silver syndrome: anaesthetic implications and management. West Indian Med. J. 55, 127–129 (2006).
Kotilainen, J. et al. Craniofacial and dental characteristics of Silver–Russell syndrome. Am. J. Med. Genet. 56, 229–236 (1995).
Canada, N. L., Mullins, L., Pearo, B. & Spoede, E. Optimizing perioperative nutrition in pediatric populations. Nutr. Clin. Pract. 31, 49–58 (2016).
Ranke, M. B. & Lindberg, A. Height at start, first-year growth response and cause of shortness at birth are major determinants of adult height outcomes of short children born small for gestational age and Silver–Russell syndrome treated with growth hormone: analysis of data from KIGS. Horm. Res. Paediatr. 74, 259–266 (2010).
Chernausek, S. D., Breen, T. J. & Frank, G. R. Linear growth in response to growth hormone treatment in children with short stature associated with intrauterine growth retardation: the National Cooperative Growth Study experience. J. Pediatr. 128, S22–S27 (1996).
Albertsson-Wikland, K. Growth hormone secretion and growth hormone treatment in children with intrauterine growth retardation. Swedish Paediatric Study Group Growth Hormone Treatment. Acta Paediatr. Scand. Suppl. 349, 35–41 (1989).
Jensen, R. B. et al. A randomised controlled trial evaluating IGF1 titration in contrast to current GH dosing strategies in children born small for gestational age: the North European Small-for-Gestational-Age Study. Eur. J. Endocrinol. 171, 509–518 (2014).
Azcona, C., Albanese, A., Bareille, P. & Stanhope, R. Growth hormone treatment in growth hormone-sufficient and -insufficient children with intrauterine growth retardation/Russell–Silver syndrome. Horm. Res. 50, 22–27 (1998).
Albertsson-Wikland, K. & Karlberg, J. Postnatal growth of children born small for gestational age. Acta Paediatr. Suppl. 423, 193–195 (1997).
Toumba, M., Albanese, A., Azcona, C. & Stanhope, R. Effect of long-term growth hormone treatment on final height of children with Russell–Silver syndrome. Horm. Res. Paediatr. 74, 212–217 (2010).
Binder, G. et al. Adult height and epigenotype in children with Silver–Russell syndrome treated with GH. Horm. Res. Paediatr. 80, 193–200 (2013).
Rakover, Y. et al. Growth hormone therapy in Silver Russell syndrome: 5 years experience of the Australian and New Zealand Growth database (OZGROW). Eur. J. Pediatr. 155, 851–857 (1996).
Clayton, P. E. et al. Management of the child born small for gestational age through to adulthood: a consensus statement of the International Societies of Pediatric Endocrinology and the Growth Hormone Research Society. J. Clin. Endocrinol. Metab. 92, 804–810 (2007).
Willemsen, R. H. et al. Long-term effects of growth hormone (GH) treatment on body composition and bone mineral density in short children born small-for-gestational-age: six-year follow-up of a randomized controlled GH trial. Clin. Endocrinol. (Oxf.) 67, 485–492 (2007).
Whitman, B. et al. Growth hormone improves body composition and motor development in infants with Prader–Willi syndrome after six months. J. Pediatr. Endocrinol. Metab. 17, 591–600 (2004).
Myers, S. E. et al. Two years of growth hormone therapy in young children with Prader–Willi syndrome: physical and neurodevelopmental benefits. Am. J. Med. Genet. A 143A, 443–448 (2007).
Ackland, F. M. et al. Physiological growth hormone secretion in children with short stature and intra-uterine growth retardation. Horm. Res. 30, 241–245 (1988).
Dufourg, M. N. et al. Silver Russell syndrome: a cause of partial IGF1 resistance? Horm. Res. Paediatr. 84, 235 (2015).
Saenger, P., Czernichow, P., Hughes, I. & Reiter, E. O. Small for gestational age: short stature and beyond. Endocr. Rev. 28, 219–251 (2007).
Tanner, J. M., Lejarraga, H. & Cameron, N. The natural history of the Silver–Russell syndrome: a longitudinal study of thirty-nine cases. Pediatr. Res. 9, 611–623 (1975).
Latronico, A. C., Brito, V. N. & Carel, J. C. Causes, diagnosis, and treatment of central precocious puberty. Lancet Diabetes Endocrinol. 4, 265–274 (2016).
Boonstra, V., van Pareren, Y., Mulder, P. & Hokken-Koelega, A. Puberty in growth hormone-treated children born small for gestational age (SGA). J. Clin. Endocrinol. Metab. 88, 5753–5758 (2003).
Vu-Hong, T. A., Rossignol, S., Chivu, O., Cabrol, S. & Netchine, I. Aggressive adrenarche in Silver–Russell Syndrome compromises final height despite GH treatment. Horm. Res. Paediatr. 76 (Suppl. 2), 234 (2011).
Verkauskiene, R., Petraitiene, I. & Albertsson Wikland, K. Puberty in children born small for gestational age. Horm. Res. Paediatr. 80, 69–77 (2013).
Leunissen, R. W. et al. Fat mass accumulation during childhood determines insulin sensitivity in early adulthood. J. Clin. Endocrinol. Metab. 93, 445–451 (2008).
Leunissen, R. W., Kerkhof, G. F., Stijnen, T. & Hokken-Koelega, A. Timing and tempo of first-year rapid growth in relation to cardiovascular and metabolic risk profile in early adulthood. JAMA 301, 2234–2242 (2009).
van der Steen, M. et al. Metabolic health in short children born small for gestational age treated with growth hormone and gonadotropin-releasing hormone analog: results of a randomized, dose-response trial. J. Clin. Endocrinol. Metab. 100, 3725–3734 (2015).
Lem, A. J. et al. Adult height in short children born SGA treated with growth hormone and gonadotropin releasing hormone analog: results of a randomized, dose-response GH trial. J. Clin. Endocrinol. Metab. 97, 4096–4105 (2012).
Wit, J. M., Hero, M. & Nunez, S. B. Aromatase inhibitors in pediatrics. Nat. Rev. Endocrinol. 8, 135–147 (2012).
US National Library of Medicine. ClinicalTrials.gov https://clinicaltrials.gov/ct2/show/NCT01520467 (2016).
Barker, D. J., Winter, P. D., Osmond, C., Margetts, B. & Simmonds, S. J. Weight in infancy and death from ischaemic heart disease. Lancet 2, 577–580 (1989).
Rich-Edwards, J. W. et al. Birth weight and risk of cardiovascular disease in a cohort of women followed up since 1976. BMJ 315, 396–400 (1997).
Martyn, C. N., Barker, D. J. & Osmond, C. Mothers' pelvic size, fetal growth, and death from stroke and coronary heart disease in men in the UK. Lancet 348, 1264–1268 (1996).
Newsome, C. A. et al. Is birth weight related to later glucose and insulin metabolism? — A systematic review. Diabet Med. 20, 339–348 (2003).
Lauren, L. et al. Relationship between birthweight and blood lipid concentrations in later life: evidence from the existing literature. Int. J. Epidemiol. 32, 862–876 (2003).
Huxley, R. et al. Birth weight and subsequent cholesterol levels: exploration of the “fetal origins” hypothesis. JAMA 292, 2755–2764 (2004).
Huxley, R. R., Shiell, A. W. & Law, C. M. The role of size at birth and postnatal catch-up growth in determining systolic blood pressure: a systematic review of the literature. J. Hypertens. 18, 815–831 (2000).
Ong, K. K. & Loos, R. J. Rapid infancy weight gain and subsequent obesity: systematic reviews and hopeful suggestions. Acta Paediatr. 95, 904–908 (2006).
Leunissen, R. W., Kerkhof, G. F., Stijnen, T. & Hokken-Koelega, A. C. Effect of birth size and catch-up growth on adult blood pressure and carotid intima-media thickness. Horm. Res. Paediatr. 77, 394–401 (2012).
Milovanovic, I. et al. SGA children with moderate catch-up growth are showing the impaired insulin secretion at the age of 4. PLoS ONE 9, e100337 (2014).
Veening, M. A., Van Weissenbruch, M. M. & Delemarre-Van De Waal, H. A. Glucose tolerance, insulin sensitivity, and insulin secretion in children born small for gestational age. J. Clin. Endocrinol. Metab. 87, 4657–4661 (2002).
Takenouchi, T., Awazu, M., Eggermann, T. & Kosaki, K. Adult phenotype of Russell–Silver syndrome: a molecular support for Barker–Brenner's theory. Congenit. Anom. (Kyoto) 55, 167–169 (2015).
Searle, C. & Johnson, D. Russel–Silver syndrome: a historical note and comment on an older adult. Am. J. Med. Genet. A170A, 466–470 (2016).
Sas, T., Mulder, P. & Hokken-Koelega, A. Body composition, blood pressure, and lipid metabolism before and during long-term growth hormone (GH) treatment in children with short stature born small for gestational age either with or without GH deficiency. J. Clin. Endocrinol. Metab. 85, 3786–3792 (2000).
Van Pareren, Y. et al. Effect of discontinuation of growth hormone treatment on risk factors for cardiovascular disease in adolescents born small for gestational age. J. Clin. Endocrinol. Metab. 88, 347–353 (2003).
Hokken-Koelega, A. C., De Waal, W. J., Sas, T. C., Van Pareren, Y. & Arends, N. J. Small for gestational age (SGA): endocrine and metabolic consequences and effects of growth hormone treatment. J. Pediatr. Endocrinol. Metab. 17 (Suppl. 3), 463–469 (2004).
Jensen, R. B. et al. Baseline IGF-I levels determine insulin secretion and insulin sensitivity during the first year on growth hormone therapy in children born small for gestational age. Results from a North European Multicentre Study (NESGAS). Horm. Res. Paediatr. 80, 38–46 (2013).
Feuk, L. et al. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am. J. Hum. Genet. 79, 965–972 (2006).
Augustine, E. F., Blackburn, J., Pellegrino, J. E., Miller, R. & Mink, J. W. Myoclonus-dystonia syndrome associated with Russell Silver syndrome. Mov. Disord. 28, 841–842 (2013).
Sheridan, M. B. et al. Myoclonus-dystonia and Silver–Russell syndrome resulting from maternal uniparental disomy of chromosome 7. Clin. Genet. 84, 368–372 (2013).
Rizzo, V., Traggiai, C. & Stanhope, R. Growth hormone treatment does not alter lower limb asymmetry in children with Russell–Silver syndrome. Horm. Res. 56, 114–116 (2001).
Goldman, V., McCoy, T. H., Harbison, M. D., Fragomen, A. T. & Rozbruch, S. R. Limb lengthening in children with Russell–Silver syndrome: a comparison to other etiologies. J. Child. Orthop. 7, 151–156 (2013).
Abraham, E., Altiok, H. & Lubicky, J. P. Musculoskeletal manifestations of Russell–Silver syndrome. J. Pediatr. Orthop. 24, 552–564 (2004).
Yamaguchi, K. T., Salem, J. B., Myung, K. S., Romero, A. N. & Skaggs, D. L. Spinal deformity in Russell–Silver syndrome. Spine Deform. 3, 95–97 (2015).
Farber, R. S. & Kerrigan, J. R. The multiple indications for growth hormone treatment of pediatric patients. Pediatr. Ann. 35, 926–932 (2006).
de Lind van Wijngaarden, R. F. et al. Randomized controlled trial to investigate the effects of growth hormone treatment on scoliosis in children with Prader–Willi syndrome. J. Clin. Endocrinol. Metab. 94, 1274–1280 (2009).
Bergman, A., Kjellberg, H. & Dahlgren, J. Craniofacial morphology and dental age in children with Silver–Russell syndrome. Orthod. Craniofac. Res. 6, 54–62 (2003).
Cullen, C. L. & Wesley, R. K. Russell–Silver syndrome: microdontia and other pertinent oral findings. ASDC J. Dent. Child. 54, 201–204 (1987).
Hodge, N., Evans, C. A., Simmons, K. E., Fadavi, S. & Viana, G. Occlusal characteristics of individuals with growth hormone deficiency, idiopathic short stature, and Russell–Silver syndrome. J. Dent. Child. (Chic.) 82, 135–140 (2015).
Kisnisci, R. S., Fowel, S. D. & Epker, B. N. Distraction osteogenesis in Silver Russell syndrome to expand the mandible. Am. J. Orthod. Dentofacial Orthop. 116, 25–30 (1999).
Metzler, P., Obwegeser, J. A., Jacobsen, C. & Zemann, W. Anterior alveolar segmental osteodistraction with a bone-borne device: clinical and radiographic evaluation. J. Oral Maxillofac. Surg. 70, 2549–2558 (2012).
Giabicani, E., Boule, M., Galliani, E. & Netchine, I. Sleep apneas in Silver Russell syndrome: a constant finding. Horm. Res. Paediatr. 84 (Suppl. 1), 262 (2015).
Abraham, M. B. et al. Report and review of described associations of Mayer–Rokitansky–Kuster–Hauser syndrome and Silver–Russell syndrome. J. Paediatr. Child Health 51, 555–560 (2015).
Bellver-Pradas, J. et al. Silver–Russell syndrome associated to Mayer–Rokitansky–Kuster–Hauser syndrome, diabetes and hirsutism. Arch. Gynecol. Obstet. 265, 155–157 (2001).
Ghanim, M. et al. Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver–Russell syndrome. Am. J. Med. Genet. A 161A, 572–577 (2013).
Gluckman, P. D., Hanson, M. A., Cooper, C. & Thornburg, K. L. Effect of in utero and early-life conditions on adult health and disease. N. Engl. J. Med. 359, 61–73 (2008).
Ryan, T. D. et al. Dilated cardiomyopathy in a 32-year-old woman with Russell–Silver syndrome. Cardiovasc. Pathol. 23, 21–27 (2014).
Sheridan, C. Intrauterine growth restriction — diagnosis and management. Aust. Fam. Physician 34, 717–723 (2005).
Hark, A. T. et al. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus. Nature 405, 486–489 (2000).
Bell, A. C. & Felsenfeld, G. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 405, 482–485 (2000).
Allanson, J. E. et al. Elements of morphology: standard terminology for the head and face. Am. J. Med. Genet. A149A, 6–28 (2009).
This consensus was organised by the European Network of Human Congenital Imprinting Disorders (EUCID.net) with the support of COST (European Cooperation in Science and Technology, BM1208), European Society of Paediatric Endocrinology (ESPE), Asia Pacific Paediatric Endocrine Society (APPES), Sociedad Latinoamericana de Endocrinología Pediátrica (SLEP), Pediatric Endocrine Society (PES) and other expert participants. The consensus was financially supported by the above societies and networks and did not receive funding from pharmaceutical companies. The authors would like to acknowledge the assistance of Jenny Child and Nick Child (Child Growth Foundation), Nonjia Rosen (Association Libre d'Informations sur la Croissance des Enfants 'Silver Russell'), Bénédicte Perrotin (Association FrançaIses des Familles ayant un enfant atteint du Syndrome Silver Russell (SSR) ou né Petit pour l'Age Gestationnel (PAG) et leurs amis: AFIF-SSR-PAG) and Dayna Carney (MAGIC foundation) in preparing this manuscript. Oluwakemi Lokulo-Sodipe was funded by the UK National Institute for Health Research - Research for Patient Benefit programme PB-PG-1111-26003 – VTC.
J.H.D. has received a travel bursary from Merck. B.D. has received honoraria from Fresenius Kiabi. A.G. has received financial support in respect of membership of the steering committee, Pfizer International Growth study (KIGS) database. A.H.-K. has received independent research funding for investigator-initiated and responsible studies, from Novo Nordisk Netherlands and Pfizer. A.L. has received consultancy fees from Sandoz-Alexion. K.M. has received research funding from Pfizer for SRS registry. P.M. has received consultancy fees from Novo Nordisk. S.O'C. has received speaker's fee from Pfizer Healthcare. G.B. has received consultancy fees from Novo Nordisk and Pfizer, as well as honoraria from Pfizer. The other authors declare no competing interests.
Frequency of clinical features in patients with SRS and SGA (PDF 232 kb)
Genetic variants on chromosome 11p15 (PDF 232 kb)
Genetic variants on chromosome 7 (PDF 152 kb)
Adult height data in SRS patients untreated with GH (PDF 128 kb)
Summary of recommendations (PDF 1379 kb)
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Wakeling, E., Brioude, F., Lokulo-Sodipe, O. et al. Diagnosis and management of Silver–Russell syndrome: first international consensus statement. Nat Rev Endocrinol 13, 105–124 (2017). https://doi.org/10.1038/nrendo.2016.138
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