Amaurosis congenita of Leber, 3 (medical condition)

A rare inherited retinal disease (retinal dystrophy) that starts during the fetal stage. Vision impairment is obvious at birth or within months of birth. Type 3 is distinguished from the other forms of this condition by the genetic origin of the defect – chromosome 14q23.3, RDH12 gene. See also Amaurosis congenita of Leber, type 3