PRPH2 and severe early-childhood-onset retinal dystrophy: The most important differential diagnoses of atrophic late AMD are the gene ABCA4, PRPH2, and BEST1 inherited macular dystrophies [138], including Stargardt disease (STGD1), Best disease (BD), or pseudo-Stargardt multifocal pattern dystrophy (PSPD) in late atrophic stages [139].