MeSH Browser

MeSH Supplementary: Chorioretinal atrophy, progressive bifocal
Unique ID: C535356
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535356
Entry Term(s): CRAPB Chorioretinal atrophy progressive bifocal; PBCRA Progressive bifocal chorioretinal atrophy; Progressive bifocal chorioretinal atrophy
Registry Number: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary
Frequency: 45
Note: A rare, autosomal dominant congenital chorioretinal dystrophy. The disorder is characterized by progressive macular and nasal retinal atrophic lesions, NYSTAGMUS; MYOPIA, and poor vision There are 2 distinct foci of atrophy, a temporal focus that is present at birth and a nasal focus that appears early in life. RETINAL DETACHMENT is an additional complication of the disease. OMIM: 600790
Date of Entry: 2010/08/25
Revision Date: 2019/06/19

Chorioretinal atrophy, progressive bifocal MeSH Supplementary Concept Data 2024