Gyrate atrophy of the choroid and retina (GACR) is a rare inborn error of amino acid
metabolism caused by bi-allelic variations in OAT. GACR is characterised by vision decline …

Gyrate atrophy (GA) of the choroid and retina is a rare autosomal recessive genetic
condition characterized by elevation of the plasma level of the amino acid ornithine due to …

Background To evaluate the relationship between superficial, deep foveal avascular zone
(FAZ) and foveal cyst areas in eyes with cystoid macular oedema (CMO) associated with …

Background: Gyrate atrophy of the choroid and retina is a rare autosomal recessive
condition characterized by chorioretinal atrophy due to deficiency of the enzyme ornithine …

Optical coherence tomography angiography (OCT-A) is a valuable imaging technique,
allowing non-invasive, depth-resolved, motion-contrast, high-resolution images of both …

Gyrate Atrophy Of The Choroid and Retina - Abstract - Europe PMC Sign in | Create an account
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Ornithine aminotransferase (OAT) deficiency is an autosomal recessive disease
characterized by elevated serum ornithine levels caused by mutations in genes encoding for …

Purpose: To evaluate the use of intravitreal bevacizumab injections for the treatment of
intraretinal cystic spaces associated with gyrate atrophy of the choroid and retina. Methods …

Gyrate atrophy of the choroid and retina (GACR) is a rare autosomal recessive disease
characterised by elevated plasma ornithine levels due to deficiency of the enzyme ornithine …

Cystoid macular oedema (CMO), which is defined as a macular thickening and cystic
changes due to accumulation of fluid, could be asymptomatic and only diagnosed using …