Typical presentation of autosomal recessive oculocutaneous albinism in two siblings

Typical presentation of autosomal recessive oculocutaneous albinism in two siblings

Objective: We report the case history and clinical findings in two siblings, a 13-year-old male and a 10-year-old female, who presented with complaints of poor vision since childhood. Both children had blonde hair and depigmented skin. Methods: Ocular examination revealed white eyebrows, white eyel...

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Bibliographic Details
Main Authors: Nishant, Prateek, Aftab, Naila, Saha, Bhawesh, Raj, Amit
Format: Article
Language:English
Published: German Medical Science GMS Publishing House 2025-04-01
Series:GMS Ophthalmology Cases
Subjects:
fovea centralis
hypomelanosis
iris
low vision
melanin
Online Access:https://journals.publisso.de/en/journals/oc/volume15/oc000249
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