A recent study reported a heterozygous c.124T>C (p. Trp42Arg) mutation in the first thrombospondin type 1 (TSR) motif of ADAMTSL1, which is responsible for a complex disorder with features including developmental glaucoma, myopia, and/or retinal defects (Hendee et al., 2017). This evidence concerns the gene ADAMTSL1 and myopia.