Mutations in the ABCA4 (gene ID: 24; OMIM: 601691) gene have been described in ABCA4-associated retinopathies, including STGD1, cone-rod dystrophy (CRD), retinitis pigmentosa (RP), and retinal dystrophy [1, 5]. This evidence concerns the gene ABCA4 and Retinal dystrophy.