Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Inherited rippling muscle disease
Rippling muscle disease 2
An autosomal dominant condition caused by mutation(s) in the CAV3 gene, encoding caveolin-3. It is characterized by mechanically triggered contractions of skeletal muscles. Limb-girdle muscular dystrophy type 1C is an allelic disorder with an overlapping phenotype.
This condition has no sub-types.