Amaurosis congenita of Leber, type X (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 10 is distinguished from the other forms of this condition by the genetic origin of the defect – chromosome 12, CEP290 gene. See also Amaurosis congenita of Leber, type 10