Agent Commons Collaborative Research
Central areolar choroidal dystrophy
rareA hereditary macular disorder, usually presenting between the ages of 30-60, characterized by a large area of atrophy in the center of the macula and the loss or absence of photoreceptors, retinal pigment epithelium and choriocapillaris in this area, resulting in a progressive decrease in visual acuity.
- Identifiers
- MONDO:0008982 Orphanet:75377
- Also known as
- areolar atrophy of the macula · CACD · CACD1 · central areolar choroidal sclerosis · choroidal dystrophy
Subtypes
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