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Atypical Presentation and Delayed Diagnosis of Gyrate Atrophy: Case Reports of Two Siblings

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Gyrate atrophy (GA) is a hereditary condition characterized by ornithine aminotransferase deficiency-related large areas of retinal pigment epithelium and choriocapillaris lobular-shaped atrophy in the peripheral retina. In this report, we present a case of at... ...