Fig. 1: Color fundus photographs of four patients with Leber’s congenital amaurosis (LCA) caused by RPGRIP1 mutations.
From: Retinal structure in Leber’s congenital amaurosis caused by RPGRIP1 mutations
Fundus photographs of both eyes show attenuated retinal vessels (arrowheads) in cases 1–3 (EYE20, 64, and 65). In the photographs for case 4 (EYE55), the fundus lacks the typical changes seen in LCA
