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Charcot-Marie-Tooth Disease

Also called: Hereditary motor and sensory neuropathy, Peroneal muscular atrophy 
 
 

Charcot-Marie-Tooth disease (CMT) is a group of genetic nerve disorders. It is named after the three doctors who first identified it. In the United States, CMT affects about 1 in 3,300 people.

CMT affects your peripheral nerves. Peripheral nerves carry movement and sensation signals between the brain and spinal cord and the rest of the body. Symptoms usually start around the teen years. Foot problems such as high arches or hammertoes can be early symptoms. As CMT progresses, your lower legs may weaken. Later, your hands may also become weak.

There is no cure. The disease can be so mild you don't realize you have it or severe enough to make you weak. Many people with CMT lead active lives and have a normal life span. Physical therapy, occupational therapy, braces and other devices and sometimes surgery can help you cope.

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Illustration of the nervous system, including brain, spinal cord, and peripheral nerves

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National Institutes of Health