Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Muscular dystrophy-dystroglycanopathy, type B
Muscular dystrophy-dystroglycanopathy type B6
A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with mental retardation and structural brain abnormalities that has material basis in homozygous or compound heterozygous mutation in the LARGE gene on chromosome 22q12.
This condition has no sub-types.