We review ocular motor cranial nerve palsies in childhood and highlight many of the features that differentiate these from their occurrence in adulthood. The clinical characteristics of cranial nerve palsies in childhood are affected by the child’s impressive ability to repair and regenerate after injury. Thus, aberrant regeneration is very common after congenital III palsy; Duane syndrome, the result of early repair after congenital VI palsy, is invariably associated with retraction of the globe in adduction related to the innervation of the lateral rectus by the III nerve causing co-contraction in adduction. Clinical features that may be of concern in adulthood may not be relevant in childhood; whereas the presence of mydriasis in III palsy suggests a compressive aetiology in adults, this is not the case in children. However, the frequency of associated CNS abnormalities in III palsy and the risk of tumour in VI palsy can be indications for early neuroimaging depending on presenting features elicited through a careful history and clinical examination. The latter should include the neighbouring cranial nerves. We discuss the impact of our evolving knowledge of congenital cranial dysinnervation syndromes on this field.
Palsies of cranial nerves III, IV, and VI are rare in childhood, with an estimated incidence of 7.6 per 100 000.1 The affected child differs from the adult in several ways. In the presence of cranial nerve paresis, the child’s developing visual system is liable to develop strabismic, deprivation, or anisometropic amblyopia. Fusion and stereopsis may be reduced or abolished. The child also differs from the adult in his/her impressive ability for repair, altering the clinical presentation of cranial nerve paresis in childhood. In this brief review of cranial nerve paresis in childhood we highlight some of these differences.
We previously reported our experience with IIIrd nerve palsy in children,2 a series of 18 children presenting under 15 years of age. The causes are shown in Table 1. As in other larger pediatric series,3 congenital and trauma were the most common aetiological factors. The frequency of associated neurological abnormalities (arachnoid cyst, optic nerve hypoplasia, and so on) supported the recommendation of neuroimaging of all children presenting with congenital or acquired cranial nerve III palsy. Notable features in our series were the almost universal presence of aberrant regeneration because of misrouting of regenerating III fibres in congenital palsy (5 of 6 (83%)) and the frequent presence of pupil involvement that, in contrast to the adult, did not suggest an increased likelihood of a compressive aetiology. As in Adie’s pupil, symptomatic mydriasis can be treated with Pilocarpine 0.1% drops in the affected eye. In addition, like Adie’s pupil, the mydriatic pupil of III palsy is frequently observed to become miotic, often over a period of years.
Congenital III palsy may present with complete ptosis and ophthalmoplegia or a partial palsy with or without aberrant regeneration. The degree of paralysis and subsequent recovery determines the likelihood of achieving a reasonable visual acuity in the affected eye; satisfactory alignment with the use of an anomalous head posture may be associated with a good visual outcome. This was the case in 6 of our patients (33%). Other important amblyogenic factors include reduced accommodation in the affected eye. In the presence of underlying hypermetropia, so common in children, this is equivalent to penalization of the affected eye. Correction of the hypermetropia and use of a bifocal lens for near is helpful, along with an appropriate occlusion regime for the contralateral eye.
A congenital or acquired III palsy with subsequent repair and aberrant regeneration should be distinguished from the much more worrying history of a previously normal child who has slowly (often over a period of years) developed a III palsy, with progressive ptosis and exotropia (with or without pupil signs) but who has evidence of aberrant regeneration. The temporal pattern of this ‘primary aberrant regeneration’ should alert the clinician to the possibility of nerve damage from a compressive process with simultaneous ongoing repair. This is a classical sign of a slow-growing lesion in the cavernous sinus such as a schwannoma or meningioma.4 The corneal sensation may also be decreased indicating concurrent Vth nerve involvement. This clinical scenario should prompt magnetic resonance imaging (MRI) of the brain with particular attention to the cavernous sinus. Neurofibromatosis 2, a tumour-suppressor mutation, has a relative predilection for tumour formation in cranial nerves III and V, probably because of their relative bulk compared with cranial nerves IV and VI.
Rarely, repair does not result in resolution of III palsy with or without aberrant regeneration. Instead, children with oculomotor nerve paresis with cyclic spasms have a history of unilateral congenital III palsy with ptosis, esotropia, and mydriasis. Every 2 min or so, bursts of III function result in elevation of the ptotic eyelid as the globe starts to adduct and the pupil constricts. This ‘spastic phase’ lasts ∼30 s before III function reverts to the ‘paretic phase’.5 This condition, sometimes also known as ‘Cyclical III palsy’, likely results from disrupted repair processes following congenital III; Miller6 demonstrated very similar findings in two adults who had previously undergone skull-base irradiation with subsequent repair, a process that the author felt was similar to the development of neuromyotonia.
In recent years, there has been a rapid evolution in our understanding of the disorders formerly known as congenital fibrosis of the extraocular muscles. These disorders, identified as CFEOM 1–3, resulted in variable manifestations of ptosis with vertical movement deficits and reduction of horizontal eye movements. Pupillary signs are occasionally evident as these disorders reflect variable congenital involvement of the III nerve. We examined an affected infant under general anaesthesia at the age of 10 months and noted free forced duction testing. The same examination repeated in this patient at the age of 9 years showed marked restriction, particularly in elevation. ‘Congenital Fibrosis’ is thus a misnomer as the restrictive ‘fibrosis’ is a feature that develops secondary to disuse related to primary congenital dysinnervation.
The phenotypic patterns were named CFEOM 1–3, but as is often the case in pediatric ophthalmology, the underlying genetic mutations that arise anywhere from the brainstem to the orbit are forcing a rethink of this group of conditions that are now referred to as the congenital cranial dysinnervation disorders (CCDDs)7, 8
Fourth (trochlear) nerve palsy is the commonest congenital cranial nerve palsy.1 Physically slender, with a long intracranial course, this nerve is subject to traumatic damage. Unilateral or bilateral fourth nerve palsy results in characteristic motility patterns including elevation in adduction, V-pattern related to reduced abduction force in downgaze with unopposed adduction by the inferior recti, and excyclotorsion. Chin-down head posture for bilateral and contralateral head tilt for unilateral palsy are noted, and the diagnosis is made clinically with support from orthoptic testing that reveals large vertical fusional ranges for long-standing or congenital cases. Thus, neuroimaging is rarely indicated.
However, several imitators exist. In particular, the craniofacial disorders are known to produce ocular motility patterns that are virtually identical. Some patients may also present with this characteristic ocular motility pattern without overt craniofacial signs (Figure 1). In the presence of an unexplained primary V-pattern with bilateral superior oblique underaction or, conversely, a primary A-pattern with bilateral superior oblique overaction, we recommend a careful examination of the lid fissure, as a marked mongoloid or anti-mongoloid slant may be the only indicator of underlying ex- or in-cyclo rotation of the orbital contents as seen in craniofacial disorders. An accompanying oblique astigmatism may confirm this entity. Coronal cuts on orbital MRI will highlight the lateral displacement of the superior recti and medial displacement of the inferior recti, superior displacement of the medial recti, and inferior shift of the lateral recti, emphasizing the orbital cause of this primary V-pattern ocular motility disorder. An analogous condition has been described with primary A-pattern with incyclotorsion of the orbital contents.9
Fourth nerve palsy imitations frequently go undetected. Occasionally a Superior oblique tendon is found at surgery to be completely absent.10 In the past few years, radiological techniques using higher-resolution 3T MRI have been used to identify the fourth nerve in normal patients and those with congenital fourth nerve palsy.11 A total of 97 patients with a history consistent with congenital IV nerve palsy were reviewed: the ipsilateral IVth nerve was absent in 73% of patients, with variable ipsilateral superior oblique hypoplasia. The authors suggested that congenital IVth nerve palsy, a common and unexplained form of congenital cranial nerve paresis, was also a form of CCDD.
Knapp12 wrote a classic series of papers regarding the surgical management of IVth nerve palsy, emphasizing the importance of careful preoperative measurements, tailoring surgery to the gaze direction in which the deviation is greatest through judicious use of rectus recessions, inferior oblique weakening, and superior oblique tuck.
Fells and his team13 reviewed the management of bilateral superior oblique palsy and stressed the importance of dealing with any significant torsion as a primary procedure, using his modification of the Harada Ito procedure. Failure to deal with the torsion was an important barrier to a satisfactory fusion result in this series. Identification of masked bilaterality and appropriate planning for torsional correction are important in preoperative surgical planning for bilateral IVth nerve palsy.
Lee et al14 reported a series of 75 children with VIth nerve palsy, all of whom had undergone neuroimaging. (Table 2) They found that almost half of the cases were due to neoplasm and suggested that neuroimaging should be considered. Conversely, Holmes et al1 in their population-based review of cranial nerve palsies in children found that no case of intracranial neoplasia presented as an isolated cranial nerve palsy. We recommend neuroimaging for the majority of cases, particularly if there is involvement of the neighbouring cranial nerves. Illustrative patients (Figures 2 and 3) are reminders that the VIth and Vth nerves are contiguous in the cavernous sinus so that loss of corneal sensation indicates pathology at that site. Conversely, the VIth and VIIth nerves are contiguous in the pons and facial nerve weakness accompanying VI palsy points to pontine pathology.
Lee et al14 in their review of 75 children with VIth nerve palsy who had undergone neuroimaging found that 11% were congenital. In this number, they included children with Duane Syndrome; it is true that Duane and Moebius syndromes, which are both forms of CCDD, are types of congenital VIth nerve paresis; Duane syndrome is a congenital VIth nerve palsy with repair by the IIIrd nerve and Mobius syndrome may present VIth nerve palsy or a full-blown horizontal gaze palsy.
Sixth nerve palsy may complicate otitis media, an association known as Gradenigo syndrome. In addition, there may be venous or even cavernous sinus thrombosis, making this complication of otitis media potentially life-threatening.15 It is difficult to know whether the current trend to withhold antibiotics for acute otitis media is contributing to a possible increased incidence of severe complications such as those noted in our report.
Benign idiopathic VIth nerve palsy is a condition that is not uncommon in childhood; Mahoney and Liu16 reviewed 225 children with VIth nerve palsies and found that 30 (13%) were in this group. Their mean age was 3 years and 28 of the 30 had an MRI. In four of the patients, the esotropia eventually became comitant. Sturm and Schöffler17 reported a group of 12 children followed up for over 9 years. Like previous authors, they pointed out a preponderance of girls affected by a left-sided palsy that resolved in <6 months. In three of their patients, they reported an ipsilateral recurrence.
In summary, the clinical characteristics of cranial nerve palsies in childhood are modified by the child’s capacity for repair and regeneration after injury. Thus, aberrant regeneration is very common after congenital III palsy; Duane syndrome, a form of congenital VI palsy, is invariably associated with retraction of the globe in adduction related to the innervation of the lateral rectus by the III nerve causing co-contraction in adduction, another form of repair. Clinical features that may be of concern in adulthood may not be relevant in childhood; whereas the presence of mydriasis in III palsy suggests a compressive aetiology in adults, this is not the case in children. However, the frequency of associated CNS abnormalities in III palsy and the risk of tumour in VI palsy can be indications for early neuroimaging depending on presenting features elicited through a careful history and clinical examination. The latter should include the neighbouring cranial nerves.
Recent genetic and neuroradiological evidence, as well as our evolving understanding of the genetic control of the process of extraocular muscle innervation, have highlighted the clinical entity of CCDD. Increasingly, we realize that this group of disorders is an important aetiological factor underlying the congenital cranial nerve palsies.
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The authors declare no conflict of interest.
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Lyons, C., Godoy, F. & ALQahtani, E. Cranial nerve palsies in childhood. Eye 29, 246–251 (2015). https://doi.org/10.1038/eye.2014.292
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