Caveolinopathy
MONDO:0016146A group of muscle diseases with basis in CAV3, which encodes caveolin-3, a muscle-specific membrane protein and the principal component of caveolae membrane in muscle cells in vivo. It is the only gene in which pathogenic variants are known to cause caveolinopathies. Sequence analysis identifies pathogenic variants in more than 99% of affected individuals
Also known as: qualitative or quantitative defects of caveolin-3
0 clinical trials for this condition and its sub-types, 0 tagged with Caveolinopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Caveolinopathy
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.