Autosomal recessive bestrophinopathy

MONDO:0012733

Autosomal 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).

Also known as: retinopathy, Burgess-Black type, ARB, bestrophinopathy, autosomal recessive

37 clinical trials for this condition and its sub-types.

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