Leber congenital amaurosis 8

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CRB1 gene.

Also known as: CRB1 Leber congenital amaurosis, LCA8, Leber congenital amaurosis 8, Leber congenital amaurosis caused by mutation in CRB1, Leber congenital amaurosis type 8

33 clinical trials for this condition and its sub-types.