Case report describes GA-like phenotype in a child with normal ornithine levels, suggesting unique characteristics.
Gyrate atrophy (GA) is a rare autosomal recessive disorder characterized by chorioretinal dystrophy. Here, we report a rare occurrence of GA-like phenotype (GALP) in a 10 years old girl with normal blood plasma ornithine levels.
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Thakur et al. (2025) studied this question.
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