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¹Göz Kliniği, Beyoğlu Göz Eğitim ve Araştırma Hastanesi 2. Göz Kliniği
²Beyoğlu Göz Eğitim ve Araştırma Hastanesi
³Göz Kliniği, Beyoğlu Göz Eğitim ve Araştırma Hastanesi 1. Göz Kliniği Gyrate atrophy is an autosomal recessively inherited progressive metabolic and systemic disorder due to deficiency of the ornithine aminotransferase enzyme. Patients have typical retinal and choroidal lesions, cataract, high myopia and hyperornithinemia. In this study, we described our clinical approach in a case of gyrate atrophy with bilateral complicated retinal detachment. There was no previous description of a case of gyrate atrophy with complicated retinal detachmen. Keywords : Gyrate atrophy, complicated retinal detachment