Gyrate Atrophy: An Overview

Journal of the Foundations of Ophthalmology 2026

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Authors: Shahmeer Hamid
DOI: 10.48089/jfo7689100
Cited by: 0

Abstract

Gyrate atrophy of the choroid and retina is a rare, autosomal recessive metabolic disorder affecting the chorioretinal tissues. The disease is caused by mutations in the OAT gene located on chromosome 10q26, which encodes the mitochondrial enzyme ornithine aminotransferase.

Fields of Study & Subjects

Metabolism and Genetic Disorders Retinal Development and Disorders Retinal Diseases and Treatments

Publication details

Journal / source
Journal of the Foundations of Ophthalmology
Publication date
17 January 2026