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Congenital Ptosis Associated With Adduction as a Dysinnervation Disorder: A Report of a Rare Case
Ghadah Alnosair1, Hassan Alhashim2, Mustafa Alhamoud3
1Pediatric Ophthalmology and Strabismus, Dammam Medical Complex, Dammam, SAU.
Insights
A rare congenital disorder caused bilateral blepharoptosis (droopy eyelids) that worsened with eye movement in a young boy. This presentation may indicate a congenital innervation dysgenesis syndrome (CID) or congenital cranial dysinnervation disorder (CCDD).
Area of Science:
- Ophthalmology
- Neurology
- Genetics
Background:
- Blepharoptosis, or droopy eyelid, results from levator palpebrae superioris muscle or third cranial nerve dysfunction.
- Congenital cranial dysinnervation disorders (CCDDs) encompass a spectrum of conditions affecting ocular muscle innervation.
- Existing literature lacks reports on blepharoptosis associated with bilateral inferior oblique underaction.
Abstract:
The levator palpebrae superioris is the primary muscle responsible for elevation of the eyelid. This muscle is innervated by the third intracranial nerve. Any pathology affecting the muscle or the supplying nerve can lead to blepharoptosis. In this study, we share our experience of a two-year-old baby boy patient who presented with a rare congenital disorder manifested as blepharoptosis increased with adduction bilaterally with no limitation of ocular muscles action except bilateral underaction of inferior oblique muscles. To our knowledge, this unusual presentation has not been previously reported in the literature. We aim in this report to build more knowledge on such a rare clinical presentation. Based on the findings, this could be a case of congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs). CCDDs/CID is a group of conditions that includes blepharoptosis as part of their clinical presentation. This group of conditions includes Duane's retraction syndrome, congenital fibrosis of extraocular muscles, and monocular elevation defect.
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