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Home » Gene Therapy for Leber Congenital Amaurosis

Gene Therapy for Leber Congenital Amaurosis

Leber congenital amaurosis (LCA) is an inherited retinal disease that causes with severe visual impairment in infancy or early childhood. Current research on a gene transfer therapy may offer hope to people with a form of this disease.

Retinal pigment epithelial (RPE) cells stained red by RPE65 antibody Retinal pigment epithelial (RPE) cells stained red by RPE65 antibody.



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This page was last modified in April 2008