Chang Sup Lee

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Ophthalmic Surgery, Lasers and Imaging Retina Case Report Open Access Chang Sup Lee, MD; Monique Leys, MD The authors describe a family of three related individuals with a previously unreported mutation in the PRPH2 gene (C213W), which is associated with pattern dystrophy simulating fundus flavimaculatus. Four eyes later developed exudative maculopathy with choroidal neovascularization, which required injections of intravitreal anti-vascular endothelial growth factor (VEGF).