Case report on interesting cases of congenital ocular motor apraxia

Congenital ocular motor apraxia (COMA) is an uncommon disorder of ocular motility characterized by inability to initiate voluntary horizontal saccades with associated head thrusts during horizontal fixation shifts. In addition, when ocular movements typical of COMA are observed, detailed systemic and neurologic examination should be performed to rule out any associated congenital neurologic or metabolic disorder. We report two cases of COMA, a 14-year-old male with diminution of vision, esotropia, and his face turned to the right without any systemic disease, and a 9-year-old male with esotropia, no face turn, acute lymphocytic leukemia, and isolated complete agenesis of the corpus callosum. Both cases had abnormal saccadic initiation for horizontal gaze with head thrusts to take fixation. Both cases underwent Medial rectus (MR) recession, which improved face turn and strabismus, respectively.

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Publication Details

Journal
Indian Journal of Ophthalmology - Case Reports
Published
2024-10-01
DOI
https://doi.org/10.4103/ijo.ijo_3050_23
Primary Topic
Fetal and Pediatric Neurological Disorders
Type
article
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article

Case report on interesting cases of congenital ocular motor apraxia

Prakhar Kumar Singh, Tanmay Mohapatra, Sanjay Kumar Dhar, Rajiv Kumar
Indian Journal of Ophthalmology - Case Reports
Fetal and Pediatric Neurological Disorders
article

Case report on interesting cases of congenital ocular motor apraxia

Prakhar Kumar Singh, Tanmay Mohapatra, Sanjay Kumar Dhar, Rajiv Kumar
article en

Abstract

Congenital ocular motor apraxia (COMA) is an uncommon disorder of ocular motility characterized by inability to initiate voluntary horizontal saccades with associated head thrusts during horizontal fixation shifts. In addition, when ocular movements typical of COMA are observed, detailed systemic and neurologic examination should be performed to rule out any associated congenital neurologic or metabolic disorder. We report two cases of COMA, a 14-year-old male with diminution of vision, esotropia, and his face turned to the right without any systemic disease, and a 9-year-old male with esotropia, no face turn, acute lymphocytic leukemia, and isolated complete agenesis of the corpus callosum. Both cases had abnormal saccadic initiation for horizontal gaze with head thrusts to take fixation. Both cases underwent Medial rectus (MR) recession, which improved face turn and strabismus, respectively.

Indian Journal of Ophthalmology - Case ReportsVol. 4(4)
Dr. Shroff’s Charity Eye Hospital (IN), Command Hospital (IN)
Good health and well-being
Openalex Percentile: Top 70%
Fetal and Pediatric Neurological Disorders
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