Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus۲۰۲۶گزارش موردنمایه شده در PubMed
Brandon Bates, Savannah Bilberry, James Gibson, Lan Hoang, Clio Armitage Harper
چکیده
Gyrate atrophy (GA) is a rare autosomal recessive disease caused by a defect in the enzyme ornithine aminotransferase (OAT). We report a case of a 4-year-old boy with GA of the choroid and retina. Following initiation of an arginine-restricted diet and targeted supplementation, there was rapid…
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DOI: 10.1016/j.jaapos.2026.104909