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
  • Retinal Pigment Epithelial Dystrophy Central
  • Foveal Dystrophy Progressive