Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype

Purpose Despite a few recent reports of patients harboring truncating variants in NSD2, a gene considered critical for the Wolf–Hirschhorn syndrome (WHS) phenotype, the clinical spectrum associated with NSD2 pathogenic variants remains poorly understood. Methods We collected a comprehensive series of 18 unpublished patients carrying heterozygous missense, elongating, or truncating NSD2 variants; compared their clinical data to the typical WHS phenotype after pooling them with ten previously described patients; and assessed the underlying molecular mechanism by structural modeling and measuring methylation activity in vitro. Results The core NSD2-associated phenotype includes mostly mild developmental delay, prenatal-onset growth retardation, low body mass index, and characteristic facial features distinct from WHS. Patients carrying missense variants were significantly taller and had more frequent behavioral/psychological issues compared with those harboring truncating variants. Structural in silico modeling suggested interference with NSD2’s folding and function for all missense variants in known structures. In vitro testing showed reduced methylation activity and failure to reconstitute H3K36me2 in NSD2 knockout cells for most missense variants. Conclusion NSD2 loss-of-function variants lead to a distinct, rather mild phenotype partially overlapping with WHS. To avoid confusion for patients, NSD2 deficiency may be named Rauch–Steindl syndrome after the delineators of this phenotype.


INTRODUCTION
Wolf-Hirschhorn syndrome (WHS, also known as 4p-syndrome, OMIM 194190) caused by partial deletions of the short arm of chromosome 4 is one of the first microscopically recognized structural chromosomal disorders, and was named after Ulrich Wolf (Freiburg, Germany) and Kurt Hirschhorn (New York, NY, USA), who first described it in 1965. 1,2 Hallmarks of the syndrome are prenatalonset growth deficiency, microcephaly, intellectual disability (ID), epilepsy, muscular hypotonia and hypotrophy, facial clefts, congenital heart defects and other malformations, as well as a very characteristic craniofacial gestalt, often described as resembling a Greek helmet. 3 With the advent of molecular cytogenetics a number of patients with smaller deletions encompassing 4p16.3 were identified, with deletions below 3.5 Mb found to be associated with a milder phenotype without major malformations. 3 Following an observation by Dian Donnai (Manchester, UK) 4 individuals described as having Pitt-Rogers-Danks syndrome were shown to also harbor 4p16.3 microdeletions sizing at least 3.7 Mb 5 and, as pointed out by Agatino Battaglia (Pisa, Italy) and John C. Carey (Salt Lake City, UT, USA), are actually clinically indistinguishable from WHS. 6 Further refinement of the WHS critical region hinted at NSD2 (also named WHSC1 or MMSET, OMIM *602952) as the gene possibly responsible for part of the manifestations of WHS, including growth retardation, ID, and possibly susceptibility to infections. [7][8][9][10] This hypothesis was supported by a role for NSD2 in neuronal development as well as in the regulation of cellular proliferation in vitro. [11][12][13] A total of eight truncating, two splicing, and six missense variants were listed among many others in sequencing studies of patient cohorts with neurodevelopmental disorders, growth abnormality, or congenital heart defects without deep phenotyping information (Table S1).
Recently, eight individual patients with developmental delay (DD) and growth retardation carrying truncating or protein-elongating variants in NSD2 have been described, [14][15][16][17][18] with phenotypes that partially overlap with those of individuals carrying very small chromosomal deletions encompassing NSD2. [8][9][10] However, the lack of larger systematic patient series and functional validation is hampering the understanding of the phenotype associated with NSD2 constitutional variants. Here we report 18 additional deep-phenotyped individuals carrying heterozygous (likely) pathogenic NSD2 variants, including a prenatal and two familial cases, together with in silico and in vitro data providing insight into the underlying pathomechanism and genotype-phenotype correlations.

MATERIALS AND METHODS
The 18 previously undescribed patients with pathogenic NSD2 variants reported in this study were identified by research or diagnostic exome or Mendeliome sequencing in various laboratories and collected via GeneMatcher (see Web Resources). When no developmental testing was performed, the degree of ID was estimated using the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) severity levels for ID (see Web Resources). Standard deviation scores for growth parameters were calculated based on the data sets provided by the Swiss Society of Pediatrics, which combine World Health Organization, Swiss, and German population data (see Web Resources). The facial overlay Fig. 4b was obtained using the Face2Gene RESEARCH application (FDNA Inc., Boston, MA, USA) taking one frontal photo for each patient at the youngest available age.
NSD2 variant nomenclature refers to the NM_133330.2 transcript and pathogenicity classification is based on the American College of Medical Genetics and Genomics/Association for Molecular Pathology (ACMG/AMP) guidelines. 19 Structural analysis of NSD2 variants was performed using SwissModel, RasMol, and Smart (see Web Resources). While the experimental crystal structure of the NSD2 N-methyltransferase domain was available (Protein Data Bank, PDB: 5LSU), the PHD and PWWP domains were modeled using the homologous domains from TRIM24 (PDB: 4ZQL) and NSD3 (PDB code: 2DAQ), respectively.
GST fusion proteins were obtained as described in the Supplementary methods. In vitro methylation assays were performed as described in Mazur et al. 20 and the Supplemental methods using reagents listed in Table S2.
The data in Fig. 2n, p, r, t are represented as mean ± SD of two independent biological replicates; statistical significance was tested by one-way analysis of variance (ANOVA) followed by two-tailed Dunnett's test without adjusting for multiple testing. The data in Fig. 3c-e are represented as mean ± SD. Groups in Fig. 3e were compared by homoscedastic two-tailed Student's t-test after testing for equal variance by F-test.

RESULTS
We describe 18 patients, 16 of whom unrelated, carrying ultrarare (absent in gnomAD) pathogenic or likely pathogenic NSD2 variants (Table S3). Of these, 6 carried 5 different missense variants while 12 carried 10 different truncating variants. Nine of the truncating and four of the missense variants were not reported previously (Fig. 1). Variant inheritance could not be determined in 4/18 cases, and was confirmed parental in 3/18 cases and de novo in 11/18 cases. NSD2 is the principal enzyme that dimethylates histone H3 at lysine 36 (H3K36me2) 11 in most cell types and tissues. 21 H3K36me2 is an evolutionarily conserved histone modification linked to transcriptional activation. The (likely) pathogenic missense variants we found map to three distinct domains of NSD2. The Cys869Tyr (patient 1-I) substitution disrupts zinc binding within a PHD finger domain (residues 831-875) and hence induces improper folding and loss of function for this domain. Although the function of the NSD2 PHD domain is unknown, these domains are virtually always found on chromatinassociated proteins and may function as epigenetic reader domains (Fig. 2a, b). The Pro895Leu variant (patients 7-I and 7-II) is located in the core of one of NSD2's PWWP domains (Fig. 2c), another motif that generally functions as an epigenetic reader. 22 The leucine substitution at Pro895 is predicted to destabilize the domain through steric clashes with the adjacent Trp885 (Fig. 2d).
All remaining missense variants are located within the methyltransferase domain of NSD2. Lys1019Arg (patient 12-I) is E 1 0 9 9 K Y 1 1 7 9 A C 8 6 9 Y P 8 9 5 L K 1 0 1 9 R K 1 0 1 9 R E 1 0 9 1 K E 1 0 9 1 K E 1 0 9 9 K W T K 1 0 1 9 R E 1 0 9 1 K E 1 0 9 9 K S 1 1 3  located in a loop of the methyltransferase domain that exhibits high local mobility or is entirely missing in the isolated NSD2 crystal structure. This hampers reliable modeling but suggests that this region is flexible and might become stabilized upon protein-protein interactions, such as binding to the nucleosome substrate. Ser1137 is located in the domain's core ( Fig. 2e) and substitution to phenylalanine (p.Ser1137Phe, patient 10-I) is predicted to result in steric clashes with the adjacent Leu1163 residue (Fig. 2f), leading to domain destabilization. Glu1091 forms a salt bridge to Arg1160 in the wild-type structure (Fig. 2g), which is disrupted due to the charge inversion in the Glu1091Lys variant (patient 5-I, Fig. 2h). In addition, the longer Lys1091 sidechain forms steric clashes with Arg1160, which are expected to additionally destabilize the methyltransferase domain. To corroborate our in silico and in vitro data, we also tested previously functionally characterized substitutions within the methyltransferase domain, namely Glu1099Lys, Tyr1092Ala, and Tyr1179Ala. Glu1099Lys is a recurrent variant found somatically in multiple cancer types including childhood leukemia and enhances methylation activity to alter global histone methylation. 23 Molecular modeling 23 suggested that the positively charged lysine may disrupt the favorable histone-enzyme interactions leading to a gain of function. Tyr1092Ala and Tyr1179Ala were not previously identified in patients but had been shown to abrogate catalytic activity based on homology to other SET domain protein lysine methyltransferase enzymes. 11 Tyr1092 forms tight hydrophobic interactions with Leu1120 in the protein core (Fig. 2I). Due to the shorter sidechain, these interactions are lost in the Ala1092 variant ( Fig. 2j) thereby predicted to destabilize the protein domain. Modeling of the Tyr1179Ala variant reveals that Tyr1179 forms direct interactions with the bound methyl donor Sadenosylmethionine (SAM, Fig. 2k). These interactions are lost in the Tyr1179Ala mutant ( Fig. 2l), resulting in a predicted strong reduction of cofactor binding and hence loss of enzymatic activity. Based on these data, we postulated that one functional consequence of the NSD2 missense variants identified in patients with developmental disorders might be disruption of NSD2's ability to generate H3K36me2.
To test this hypothesis, we determined H3K36me2 levels in HEK293T cells transiently transfected with NSD2 wild-type or derivatives harboring the various variants (Fig. 2m, n). Consistent with previous work, 11,22 overexpression of wild-type NSD2 and a cancer-related NSD2 gain-of-function mutant (Glu1099Lys [E1099K]) 23 caused a global increase in H3K36me2. Contrarily, the NSD2 derivatives carrying variants observed in patients, apart from Cys869Tyr [C869Y] (patient 1-I) and Glu1091Lys [E1091K] (patient 5-I), significantly reduced the levels of H3K36me2 ( Fig. 2m; quantitation in Fig. 2n). In particular, Ser1137Phe [S1137F] (patient 10-I) largely behaved like the negative control and the known NSD2 catalytic mutant Tyr1179Ala [Y1179A] (Fig. 2m, n). Given that Ser1137Phe (patient 10-I) is located within the SET domain, the data suggest that this variant causes direct impairment of NSD2's catalytic activity. To test this hypothesis, in vitro methylation assays were performed using a minimal domain of NSD2 that retains enzymatic activity 11 and recombinant nucleosomes as substrates. As shown in Fig. 2o and q (quantitation in Fig. 2p and r, respectively), Ser1137Phe (patient 10-I) abrogates NSD2's ability to methylate nucleosomes in vitro similarly to the previously characterized catalytic mutant Tyr1179Ala [Y1179A]), while Glu1091Lys (patient 5-I) and Lys1019Arg [K1019R] (patient 12-I) showed a modest reduction in methylation of nucleosomes ( Fig. 2o-r). Cys869Tyr (patient 1-I) and Pro895Leu (patients 7-I and 7-II) lie outside of the minimal catalytic domain and thus could not be tested in this assay. Next, we used the CRISPR/Cas9 system to generate NSD2-depleted HT1080 cells, which leads to depletion of global H3K36me2, and then complemented these cells with CRISPR-resistant wild-type NSD2 or the DD-associated NSD2 variants to test their role in reconstituting physiologic levels of H3K36me2. In contrast to complementation with wild-type NSD2 and gain-of function NSD2-Glu1099Lys, cells complemented with the DD-associated NSD2 variants were partially to largely compromised in their ability to rescue physiologic H3K36me2 levels, with Glu1091Lys (patient 5-I) being the only variant that did not reach statistical significance (Fig. 2s, t). The Ser1137Phe variant (patient 10-I) completely failed to rescue, indicating that it essentially abolishes enzymatic activity. Overall, these data are consistent with all variants except Cys869Tyr (patient 1-I) compromising to varying degrees the ability of NSD2 to generate H3K36me2, a key epigenetic modification.
The main clinical features of the NSD2 cohort consisting of 18 individuals described here and 10 previously published individuals (8 carrying truncating or protein-elongating variants 14-18 and 2 carrying a microdeletion that encompasses the NSD2 gene only 10 ) are summarized in Fig. 3a and compared to patients with WHS due to 4p deletions of different sizes reported in a large series of 166 affected individuals 3 (Fig. 3b). Postmortem pathological findings for case 16-I, a male fetus whose pregnancy was terminated at the 27th week of gestation, are shown in Figure S1. Detailed clinical descriptions are provided in the supplement.
In the NSD2 cohort, the average age at last visit (±SD) was 9.3 (±10.3) years and the male to female ratio was 18:10 (male 64%, female 36%). Seventy-five percent of the NSD2 variants were de novo, 14% were inherited from an affected parent, while in 11% of the cases, the inheritance pattern could not be established. Patients with (likely) pathogenic NSD2 variants shared a similar facial gestalt characterized by a triangular face, broad forehead, high anterior hairline, deeply set eyes, large palpebral fissures, broad arched and laterally sparse eyebrows, periorbital hyperpigmentation, full cheeks, a thin and elevated nasal bridge, smooth short philtrum, prominent cupid bow, thick everted lower lip vermilion, and/or protruding ears (Fig. 4a, b). Noticeably, the facial appearance evolved over time, with older patients developing deeper infraorbital creases. Family 6 comprised a total of 7 clinically similarly affected individuals, with molecular confirmation available for four of them, and represents to date the largest known family affected by this disorder (Fig. 4c). The core phenotype of the NSD2 cohort (>50% of patients) is characterized by DD, intrauterine growth retardation and low birth weight, feeding difficulties, failure to thrive, height and head circumference below the 5th centile (<−1.65 SDS), speech delay, and muscular hypotonia. Although these manifestations are present in WHS as well, the majority of the individuals in the NSD2 cohort lack many of the most common manifestations of WHS such as seizures, 3 orofacial clefts, and coloboma, as well as genital, cardiac, and renal malformations and display a distinct facial phenotype that lacks the classical "Greek helmet" aspect. Furthermore, the severity of the ID in the NSD2 cohort was milder compared with patients carrying the most common 4p deletions (between 5 and 18 Mb), who are severely affected in 76% of the cases. 3 While individuals 1-I, 13-I, and 14-I harboring the NSD2 Cys869Tyr, p.Cys1183Valfs*146, and p.Arg600* variants respectively, either had an IQ in the lower-normal range (78-81 and 89, respectively) or presented with learning difficulties, individuals old enough for evaluation commonly showed mild ID, with only three individuals presenting with severe ID. The latter carried truncating variants (3-I c.3223_3226dup p.Gly1076Valfs*16; 4-1c.1588_1589dupAA p.Ile532Glyfs*67; Bernardini et al., patient 3, exon 1-20 deletion), which may not be held responsible for the severe ID. Both siblings described as patients 2 and 3 in Bernardini et al. carry in fact the same exon 1-20 deletion, with one sibling showing mild ID, while the other had autism and severe ID. 10 Behavioral and psychological issues as well as autistic features were observed in 44% and 33%, respectively, with the most frequently reported manifestations being anxiety (15%), hyperactivity (22%), and aggressiveness (11%). Individual 1-I had suicidal ideations related to his poor academic performance at the age of 11 years. Of note, all the individuals carrying missense variants presented with behavioral and psychological issues (Fig. 3a), compared to 29% of patients with truncating variants or deletions (p value = 0.0031 by two-tailed Fisher's exact test).
Growth parameters at birth were largely below the norm (Fig. 3c). Feeding difficulties were described in 52% of the affected individuals and may at least in part contribute to the failure to thrive. Short stature and growth retardation persisted later in life (Fig. 3d). Delayed bone age was detected in 6 individuals (22%). Length and occipitofrontal circumference (OFC) at birth as well as all growth parameters at last visit were normally distributed according to a D'Agostino-Pearson omnibus normality test, while birth weight was skewed toward lower values (p = 0.0002). Notably, heterozygotes for missense variants were significantly taller than patients carrying truncating variants as well as small deletions encompassing NSD2 (p = 0.03 by homoscedastic t-test after checking for comparable variance by F-test; Fig. 3e) and none of them fell below the 5th centile for height at last visit. Weight and OFC at last visit were also higher in patients carrying missense variants, although this difference was not statistically significant (p = 0.27 and 0.17, respectively). Finally, a linear regression analysis showed that older patients had significantly higher body mass index (BMI) values (r² = 0.1786, p = 0.0396; Fig. 3f).
Gastrointestinal abnormalities were also quite common (43%), with constipation representing the most frequent manifestation (26%). Ophthalmological abnormalities were observed in 29% of patients and mostly included mild refraction defects and strabismus, while no individual presented with coloboma, which is considered a recurrent feature in WHS (see Fig. 3b). One exception is represented by individual 3-I, who presented with bilateral keratoconus, retinitis pigmentosa, and optic atrophy and received a corneal transplant at the age of 32. Reanalysis of her exome data revealed three rare variants of unknown significance in RHO, KRT3, and UNC45B (Table S3), which were, however, maternally inherited and also present in her healthy sister. Skeletal and limb abnormalities were reported in 39% of the cases. Individual 12-I presented with a craniosynostosis that was surgically corrected at the age of 6 months, which may be explained by the patient's additional de novo heterozygous AGO2 variant (Table S3). Also, of note, individual 7-II presented with 11 ossified ribs and 6 non-rib-bearing lumbar vertebrae. Dental abnormalities were also quite frequent (32%). Brain and spinal cord malformations were present in 5 individuals (18%) and were mostly of minor importance except for individual 16-I, who presented with vermis hypoplasia. Less frequent manifestations among patients carrying NSD2 pathogenic variants included a history of aspiration, cardiac and renal anomalies, neonatal jaundice, sleep disturbances, hearing loss, genital abnormalities, and orofacial clefts (Table S3). Immunological abnormalities as well as recurrent infections, which represent a common morbidity and mortality cause in WHS, 24 were infrequent in the NSD2 cohort, where patient 5-I presented with latex allergy, patient 11-I with low IgA and IgG 3 levels, and patients 2-I, 11-I and Derar-1 with recurrent respiratory infections. Seizures, which are common in WHS (Fig. 3b), were reported only in individual 10-I, while individual 15-I presented subclinical electroencephalogram (EEG) abnormalities at the age of 4 4/12 years. Endocrinological abnormalities seem not to be part of the phenotypic spectrum, with only individual 5-I presenting limited signs of precocious puberty at 15 months of age, which were nonprogressive and were associated with a normal endocrine evaluation. Likewise, metabolic abnormalities were only observed in individual 2-I.

DISCUSSION
In this work we describe a large series of patients carrying pathogenic variants in NSD2, thus allowing delineation of the associated manifestations, which include prenatal-onset failure to thrive with all body measurements below the mean and low BMI, mild DD and muscular hypotonia, and a distinct facial gestalt. Furthermore, we provide in silico and in vitro mechanistic data showing loss of histone methylation activity as a common feature of NSD2 deficiency.
The phenotype observed in the NSD2 cohort is consistent with many of the known functions of NSD2. First, NSD2 has long been known to regulate embryonic development and body growth, (e) Comparison of the growth parameters at last visit for patients carrying missense variants (black) compared with patients carrying other variants as well as deletions encompassing NSD2 (red). *p value < 0.05 as tested by two-tailed Student's t-test. The data in (c-e) are expressed as SDS based on the respective growth charts. Lines and whiskers represent mean ± SD. (f) Linear correlation analysis between age and BMI and last visit. ASD DD/ID developmental delay/intellectual disability, IUGR intrauterine growth restriction, SC spinal cord, SGA small for gestational age.
with heterozygous Nsd2 constitutive knockout mice growing at a much slower rate compared with wild-type littermates, homozygous knockout mice dying in the first days of life, 25 and common variants showing strong (p = 10 −24 ) association with height in genome-wide association study (GWAS). 26 Recently NSD2 was shown to regulate adipose tissue development in mice by controlling the activity of the master adipogenic transcription factor peroxisome proliferator-activated receptor-γ (PPARγ). 27 Interestingly, in this work mice overexpressing the mutant histone protein H3.3K36M, an NSD2 inhibitor, resisted white adipose tissue expansion in response to a high-fat diet. These findings support the idea that the low BMI observed in the NSD2 cohort may be due to the inability of body fat to expand in response to feeding rather than a consequence of the neonatal feeding difficulties that, although observed in multiple affected individuals, disappear later in life. Furthermore, NSD2 has been shown to play a key role in promoting adipogenesis and myogenesis in precursor cells, as well as thermogenesis in brown adipose tissue and insulin sensitivity in white adipose tissue. 27 In pancreatic β-cell lines in vitro NSD2 has also been shown to promote proliferation and to regulate insulin secretion. 28 However, since diabetes has not been reported as a recurrent feature neither in our cohort nor in patients with WHS we assume that in humans, glycemic control may be maintained despite impaired NSD2 function. Likewise, some other known or supposed functions of NSD2 did not result in a recurrent phenotype in our cohort. NSD2 has been suggested to contribute to the immune defects typical of WHS by regulating the hematopoietic process at multiple stages as well as B- 29 and T-cell 30 differentiation. Nevertheless, only a minority of the patients in this series presented with recurrent infections. Also, while heterozygous Nsd2 deficient mice present with heart defects 25 and de novo variants in NSD2 were shown to associate with congenital heart malformations, 31 cardiac anomalies were present only in a minority of the individuals in this series, and, with the exception of individual 16-I, were of minor clinical importance. The low prevalence of epilepsy in this cohort is compatible with the assumption that other genes such as LETM1 are responsible for seizures in WHS. 32,33 While heterozygotes for missense variants were on average significantly taller, the overall clinical severity correlated only loosely with the measured alteration in NSD2 enzymatic function. Furthermore, for the Cys869Tyr (patient 1-I) variant, which can be categorized as likely pathogenic based on the current ACMG/AMP recommendations, 19 we did not detect significant loss of methylation activity in our in vitro assays. These data suggest that in addition to H3K36 dimethylation, other functions of NSD2 such as its genomic localization, and likely other potential genetic differences among the patients, contribute to the pathogenesis of the complex phenotypes described here. Moreover, as the missense variants that we tested did not display any obvious stability issue upon overexpression, dominant negative effects cannot be excluded. Finally, second hits or blending phenotypes with additional variants in other (known or unknown) genes associated with the clinical phenotypes described in this study could contribute to the observed clinical variability.
Patients 11-I and 15-I carried the same protein-elongating p. Pro1343Glnfs*49 variant. Although this variant occurs too distally in the messenger RNA (mRNA) sequence to induce nonsensemediated decay, its pathogenicity is supported by the fact that this variant, together with the previously described p.Glu1344-Lysfs*49 variant, 18 all occurred de novo in similarly affected individuals. Although some of the patients in this series carried additional rare variants, none of these are likely pathogenic. Individual 1-I carries a 441-kb heterozygous interstitial microduplication in 22q11.2 (hg19 (chr22:22,817,344-23,258,369) that does not contain any disease-associated genes and was inherited from his healthy father. Individual 5-I carried the recurrent 312-kb interstitial duplication at 15q11.2 (hg19: 22,770,421-23,082,328) that was inherited from her healthy mother. In a large study on the effect of copy-number variants on cognition, 136 control individuals carrying the 15q11.2 duplication performed to a similar level as population controls on all tests of cognitive function. 34 In family 7, where both mildly affected siblings (individuals 7-I and 7-II) inherited the NSD2 variant from their similarly affected mother, we additionally found that individual 7-I carries a paternally inherited 783-kb deletion at 9p13.3 (hg19: 35,487,270,255) as well as the maternally inherited GABBR2 c.1656_1657delTT, p. Cys553Hisfs*96 variant. Her father had learning disability and depression. No overlapping deletion was present in the DECIPHER database but, based on the gene content and on the family history, a modulatory role of the 9p13.3 deletion on her phenotype cannot be excluded. Except for one truncating variant described in a large sequencing study on patients with neurodevelopmental delay, 35 all GABBR2 pathogenic variants described until now in this gene are missense (source: HGMD Professional, release 2020.2, see Web Resources). This, together with the fact that her similarly affected brother (individual 7-II) did not carry the p.Cys553Hisfs*96 GABBR2 variant, speaks against a determining role on the phenotype. Individual 10-I carries a 38-kb partial HUWE1 duplication in Xp11.2, which overlaps with a recurrent polymorphic copy-number variant that does not affect the expression of HUWE1 and thus should have no effect on cognition. 36 Our study leaves unanswered questions for future research, such as the clarification of the full molecular mechanisms. This may reveal potential targets for therapeutic interventions relevant not only to patients with NSD2 deficiency, but also potentially even to patients with obesity in general.
In conclusion, our data support the concept that NSD2 loss of function is associated with a distinct phenotype that only partially overlaps with WHS and constitutes a differential diagnosis to Silver-Russell and similar syndromes. This phenotype is in line with the distinct features described in the first patient with a small deletion encompassing NSD2 by Rauch et al. 8 This patient now at age 26 years is 172 cm tall (-0.55 SDS), weighs 45-50 kg (ca. -2.5 SDS), and has a "small head." Despite his normal eating behavior, all attempts to gain weight have been unsuccessful. He has an IQ in the lower-normal range, a calm and content personality, and lives with his parents. As a reflection of the distinct facial gestalt and the greatly different disease severity, especially concerning ID, of NSD2 deficiency and contiguous gene deletions leading to WHS, which may also be important for families' and physicians' perception of the patients' prognosis, the NSD2-related disorder may be named Rauch-Steindl syndrome after the delineators of this phenotype. 8