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Tuesday, May 7, 2013

What Is Charcot-Marie-Tooth Disorder (CMT)?
Charcot-Marie-Tooth, or CMT, is the most commonly inherited peripheral neuropathy and is found worldwide among all races and ethnic groups. Discovered in 1886 by three physicians, Jean-Martin Charcot, Pierre Marie, and Howard Henry Tooth, CMT affects an estimated 2.6 million people.

Non-Contagious, Non-Fatal, Inherited Disease
CMT usually isn’t life-threatening and almost never affects brain function. It is not contagious, but it ...is hereditary and can be passed down from one generation to the next.

Connection to the Muscular Dystrophy Association (MDA)
CMT is one of 40 diseases covered by the MDA, but unlike muscular dystrophy, in which the defect is in the muscles, CMT is a disorder in which the defect is in the nerves that control the muscles.

Symptoms
CMT patients slowly lose normal use of their extremities as nerves degenerate and muscles weaken because the affected nerves no longer stimulate the muscles. Many patients also have some loss of sensory nerve functions.

Treatments
CMT doesn’t have a cure, although physical therapy, occupational therapy, and moderate physical activity are beneficial. Sometimes CMT is surgically treated.

We want to help you better understand CMT by offering advice from professionals. Click here to find answers to the most frequently asked questions and post questions and concerns that have not yet been addressed—we’ll get you in touch with the right professional

http://www.cmtausa.org/index.php?option=com_content&view=article&id=74&Itemid=162
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