HIGHLIGHTS
- What: The authors report on a patient with OA, wide intercanthal distance, foveal hypoplasia, and areas of skin hypopigmented macules.
- Who: Ocular Albinism and colleagues from the Department of Ophthalmology, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI Department of have published the research: Review began 07/27/2024 Review ended 08/12/2024 Published 08/19/2024 © Copyright, in the Journal: (JOURNAL)
SUMMARY
Ocular albinism (OA) is a hereditary eye disease characterized by a lack of pigment in the eyes, leading to various visual abnormalities. Common ocular manifestations . . .
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