Fundus photo graphs (top) and autofluorescence images (bottom) of a patient with Stargardt disease caused by a compound heterozygous mutations in ABCA4 (c.4312C>G, p.[Pro1438Ala] and c.1253T>C, p.[Phe418Ser]). The fleck-like and tassel-like changes are more apparent in the autofluorescence images.