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Gyrate Atrophy
Jan 25 2024 by Ricardo Leal Rodríguez, MD
Fundus photograph of an 11-year-old female with hyperornithinemia (932 µmol/L ) in plasma and mutation in the OAT gene (p.Asp242Argfs*6) confirming Gyrate Atrophy
Photographer: Dr Ricardo Leal Rodríguez, Instituto de Enfermedades y Cirugía Ocular, IECO , Mérida Yucatán, México
Imaging device: Triton Plus (Ver 10.16) TOPCON
Condition/keywords: gyrate atrophy, inherited retinal disease