CRX and Leber congenital amaurosis: In another study including 18 patients from 11 families, multimodal retinal imaging combined with electrophysiology identified 4 Leber congenital amaurosis (LCA), 2 retinitis pigmentosa (RP), 6 COD/CORDs, and 6 “atypical maculopathy” patients carrying the same heterozygous CRX mutation [14].