SLC38A8 and retinopathy of prematurity: This particular appearance of the fovea can be associated with conditions such as albinism, PAX6 mutation, aniridia, retinopathy of prematurity (ROP), SLC38A8 mutations, optic nerve hypoplasia, achromatopsia, and cone-rod dystrophy, but can also be found in normal children [14,17].