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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Clinical, biochemical and molecular analysis in a cohort of individuals with gyrate atrophy

Fig. 1

Clinical imaging findings from a 22-year-old patient with gyrate atrophy (case 2). A Colour fundus images demonstrating characteristic bilateral scalloped, peripheral lesions; B Fundus autofluorescence (FA) imaging demonstrating patchy hypo-autofluorescent lesions peripherally in keeping with RPE atrophy; C Optical coherence tomography (OCT) images of the macula demonstrating bilateral cystoid macular oedema, a known complication of gyrate atrophy

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