To Top

2 Advanced Search Results for: LRAT or RPE65

Rare Disease Information

NORD Rare Disease Database

Leber Congenital Amaurosis

Leber congenital amaurosis (LCA) is a rare genetic eye disorder. Affected infants are often blind at birth. Other symptoms may include crossed eyes (strabismus); rapid,...

Also known as: LCA

Retinitis Pigmentosa

Retinitis pigmentosa (RP) comprises a large group of inherited vision disorders that cause progressive degeneration of the retina (the so-called inherited retinal...

Also known as: progressive pigmentary retinopathy, rod-cone dystrophy, RP