Fig. 2: Fluorescein angiographies (FA) 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
FA of both eyes showed granular hyperfluorescence without leakage due to retinal pigment epithelium atrophy in all four patients
