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Am J Ophthalmol Case Rep
June 2022
Ophthalmic Genetics Unit, OMMA Institute, 74 Katechaki Str., 115 25, Athens, Greece.
Purpose: To present a case of two siblings with optic atrophy associated with Wolfram Syndrome.
Observations: Two young adult siblings presented with serious bilateral loss of vision and dyschromatopsia established in early adolescence. They were referred with a presumed diagnosis of Leber's Hereditary Optic Neuropathy.