Autosomal recessive bestrophinopathy

Orpha code: 139455OMIM code: 611809

Definition

A rare 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).

Disease data
Classification

Disease

Synonyms
Retinopathy, Burgess-Black type
Retinopatia, typ Burgessa i Blacka
ORPHA code
139455
OMIM code
611809
ICD10 code
H35.5
ICD11 code
-

No additional description.

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