North Carolina macular dystrophy

MONDO:0007630

North Carolina macular dystrophy (NCMD) is a non-progressive autosomal dominant macular disorder of congenital or infantile onset characterized by loss of central vision, the accumulation of drusen in the macula and atrophy of photoreceptor cells with a variable phenotype at macular examination.

Also known as: CAPE dystrophy, CAPED, MCDR1, NCMD, North Carolina macular dystrophy, North Carolina macular dystrophy, retinal 1, caped, central areolar pigment epithelial dystrophy

25 clinical trials for this condition and its sub-types, 0 tagged with North Carolina macular dystrophy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.