Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics
- PMID: 19943106
- DOI: 10.1007/s10741-009-9156-8
Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics
Abstract
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder caused by the absence of dystrophin, a sarcolemmal protein which links the cytoskeleton to the extracellular matrix by interacting with a large number of proteins. Heart failure is a classic complication of this disease. The authors review the pathogenesis and therapeutics of cardiac involvement in DMD.
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