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Muscular Dystrophy as related to Carnitine (L-Carnitine)


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Duchenne Muscular Dystrophy 

 

The muscular dystrophies are a group of genetic and hereditary muscle diseases; characterized by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue. In some forms of muscular dystrophy, cardiac and smooth muscles are affected. The muscular dystrophies are the most common hereditary diseases.

Carnitine is an amino acid responsible for transport of fatty acids into a cell's mitochondria. It is often sold as a nutritional supplement.


Muscular Dystrophy as related to Carnitine (L-Carnitine)


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October 12, 2008


Page Updated: June 12, 2007
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