Oculopalpebral synkinesis in congenital ptosis: a case series expanding the spectrum of congenital cranial dysinnervation disorders

Purpose: Oculopalpebral synkinesis is an involuntary change in eyelid position linked to eye movement, distinct from the jaw-triggered eyelid movement of the Marcus Gunn jaw-winking phenomenon (MGJWP). It is increasingly considered part of the spectrum of congenital cranial dysinnervation disorders (CCDDs), yet only isolated case reports have described it.Methods: We examined three patients with congenital ptosis whose eyelid position varied with gaze. Eye movements were documented with clinical photographs.Results: Case 1, an 8-year-old boy, had right congenital ptosis with a classic MGJWP and a monocular elevation deficit. The right ptosis worsened on levoversion, and the left upper eyelid, which had no baseline ptosis, moved intermittently up and down on adduction: a double synkinesis. Case 2, a 25-year-old woman, had severe bilateral ptosis and jerk nystagmus since birth, without MGJWP; ptosis worsened in the adducting eye and improved in the abducting eye. Case 3, a 9-year-old girl, had severe right ptosis, right exotropia of 10°, bilateral torsional nystagmus and mild bilateral limitation of elevation, with alternating blepharoptosis in a reciprocal pattern between the two eyelids. MRI of the brain was normal where reported.Conclusion: The same eyelid phenomenon can arise from different aberrant connections between the horizontal rectus muscles and the levator palpebrae superioris, with or without a trigeminal component. We propose that these cases form a distinct group of CCDDs in which synkinesis occurs without significant limitation of ocular motility. Functional MRI and genetic studies are needed to clarify the cause.

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Publication Details

Journal
Strabismus
Published
2026-10-27
DOI
https://doi.org/10.1080/09273972.2026.2754381
Primary Topic
Ophthalmology and Eye Disorders
Type
article
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article

Oculopalpebral synkinesis in congenital ptosis: a case series expanding the spectrum of congenital cranial dysinnervation disorders

Meenakshi Wadhwani, Ruchita Sontakke, Paromita Dutta, Parul Jain et al.
Strabismus
Ophthalmology and Eye Disorders
article

Oculopalpebral synkinesis in congenital ptosis: a case series expanding the spectrum of congenital cranial dysinnervation disorders

Meenakshi Wadhwani, Ruchita Sontakke, Paromita Dutta, Parul Jain, Uttam Dhaka, Samapika Priyadarsini Tripathy
article en

Abstract

Purpose: Oculopalpebral synkinesis is an involuntary change in eyelid position linked to eye movement, distinct from the jaw-triggered eyelid movement of the Marcus Gunn jaw-winking phenomenon (MGJWP). It is increasingly considered part of the spectrum of congenital cranial dysinnervation disorders (CCDDs), yet only isolated case reports have described it.Methods: We examined three patients with congenital ptosis whose eyelid position varied with gaze. Eye movements were documented with clinical photographs.Results: Case 1, an 8-year-old boy, had right congenital ptosis with a classic MGJWP and a monocular elevation deficit. The right ptosis worsened on levoversion, and the left upper eyelid, which had no baseline ptosis, moved intermittently up and down on adduction: a double synkinesis. Case 2, a 25-year-old woman, had severe bilateral ptosis and jerk nystagmus since birth, without MGJWP; ptosis worsened in the adducting eye and improved in the abducting eye. Case 3, a 9-year-old girl, had severe right ptosis, right exotropia of 10°, bilateral torsional nystagmus and mild bilateral limitation of elevation, with alternating blepharoptosis in a reciprocal pattern between the two eyelids. MRI of the brain was normal where reported.Conclusion: The same eyelid phenomenon can arise from different aberrant connections between the horizontal rectus muscles and the levator palpebrae superioris, with or without a trigeminal component. We propose that these cases form a distinct group of CCDDs in which synkinesis occurs without significant limitation of ocular motility. Functional MRI and genetic studies are needed to clarify the cause.

Strabismus
Maulana Azad Medical College (IN)
Openalex Percentile: Top 12%
Ophthalmology and Eye Disorders
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