Fig. 3From: Coat’s like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management optionsFundus Photo (OU) and OCT (OS) of the 12 year old male sibling. a, b Fundus photos showing foveal atrophy, nummular pigmentations and moderate vascular attenuation. c OCT showing decreased foveal thicknessBack to article page