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Muscular Dystrophy as related to Vitamin B6 (Pyridoxine)


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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.

The two major forms of vitamin B6 are pyridoxine and pyridoxamine. In the liver they are converted to pyridoxal 5'-phosphate (PLP) which is a cofactor in many reactions of amino acid metabolism. PLP also is necessary for the enzymatic reaction governing the release of glucose from glycogen.


Muscular Dystrophy as related to Vitamin B6 (Pyridoxine)


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August 21, 2008


Page Updated: June 12, 2007
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