A rare, hereditary, non-progressive disorder that affects the macular, causing atrophy and drusen. It presents in young people and results from chromosome 5 and 6 mutations.
Also Known As
- NCMD
- Macular Dystrophy Retinal 1 North Carolina Type
- MCDR1
- Central Areolar Pigment Epithelial Dystrophy
- CAPED
- Retinal Pigment Epithelial Dystrophy Central
- Foveal Dystrophy Progressive