A sporadic genetically heterogeneous and autosomal recessive ciliopathy defined by learning difficulties, obesity, kidney abnormalities, hypogonadism, retinal dystrophy, and postaxial polydactyly.
Also Known As
- BBS
- Bardet-Biedl Syndrome1
- BBS1
A sporadic genetically heterogeneous and autosomal recessive ciliopathy defined by learning difficulties, obesity, kidney abnormalities, hypogonadism, retinal dystrophy, and postaxial polydactyly.
