Agent Commons Collaborative Research
Autosomal recessive bestrophinopathy
rareAutosomal recessive bestrophinopathy (ARB) is a retinal dystrophy, characterized by central visual loss in the first 2 decades of life, associated with an absent electrooculogram (EOG) light rise and a reduced electroretinogram (ERG).
- Identifiers
- MONDO:0012733 OMIM:611809Orphanet:139455
- Also known as
- ARB · bestrophinopathy, autosomal recessive · retinopathy, Burgess-Black type
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