Loss of function of retinol dehydrogenase 11 causes a recessive syndrome characterized by myopathy, retinal dystrophy, juvenile cataracts, and microcephaly. - Radio FC; Tasca G; Coppens S; Chillemi G; Whalen S; Marey I; Leoni C; Onesimo R; Deconinck N; D'Amico A; Remiche G; Nascimento A; et al. (Genetics in medicine : official journal of the American College of Medical Genetics, 2026)