Amaurosis congenita of Leber, type 4: 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 4 is distinguished from the other forms of this condition by the genetic origin of the defect - chromosome 17p13.1, AIPL1 gene. More detailed information about the symptoms, causes, and treatments of Amaurosis congenita of Leber, type 4 is available below.
See full list of 6 symptoms of Amaurosis congenita of Leber, type 4
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