Congenital hereditary endothelial dystrophy type I

Congenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterized by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision.

Also known as: CHED1, CHEDI, autosomal dominant CHED, autosomal dominant congenital hereditary endothelial dystrophy, congenital hereditary endothelial dystrophy type 1

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