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NINDS Charcot-Marie-Tooth Disease Information Page

Condensed from Charcot-Marie-Tooth Disease Fact Sheet

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What is Charcot-Marie-Tooth Disease?

Charcot-Marie-Tooth disease (CMT) is one of the most common inherited neurological disorders, affecting approximately 1 in 2,500 people in the United States.  CMT,  also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy, comprises a group of disorders caused by mutations in genes that affect the normal function of the peripheral nerves.  The peripheral nerves lie outside the brain and spinal cord and supply the muscles and sensory organs in the limbs.  A typical feature includes weakness of the foot and lower leg muscles, which may result in foot drop and a high-stepped gait with frequent tripping or falling. Foot deformities, such as high arches and hammertoes (a condition in which the middle joint of a toe bends upwards), are also characteristic due to weakness of the small muscles in the feet. In addition, the lower legs may take on an "inverted champagne bottle" appearance due to the loss of muscle bulk. Later in the disease, weakness and muscle atrophy may occur in the hands, resulting in difficulty with fine motor skills. Some individuals experience pain, which can range from mild to severe.

Is there any treatment?

There is no cure for CMT, but physical therapy, occupational therapy, braces and other orthopedic devices, and orthopedic surgery can help people cope with the disabling symptoms of the disease. In addition, pain-killing drugs can be prescribed for patients who have severe pain.

What is the prognosis?

Onset of symptoms of CMT is most often in adolescence or early adulthood, however presentation may be delayed until mid-adulthood.  Progression of symptoms is very gradual.  The degeneration of motor nerves results in muscle weakness and atrophy in the extremities (arms, legs, hands, or feet), and the degeneration of sensory nerves results in a reduced ability to feel heat, cold, and pain.  There are many forms of CMT disease.  The severity of symptoms may vary greatly among individuals and some people may never realize they have the disorder. CMT is not fatal and people with most forms of CMT have a normal life expectancy.

What research is being done?

The National Institute of Neurological Disorders and Stroke (NINDS) conducts CMT research in its laboratories at the National Institutes of Health (NIH) and also supports CMT research through grants to major medical institutions across the country.   Ongoing research includes efforts to identify more of the mutant genes and proteins that cause the various disease subtypes.  This research includes studies in the laboratory to discover the mechanisms of nerve degeneration and muscle atrophy, and clinical studies to find therapies to slow down or even reverse nerve degeneration and muscle atrophy.  

NIH Patient Recruitment for Charcot-Marie-Tooth Disease Clinical Trials


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Charcot-Marie-Tooth Association (CMTA)
P.O. Box 105
Glenolden, PA 19036
Tel: 800-606-CMTA (2682)
Fax: 610-499-9267

Muscular Dystrophy Association
National Office - 222 S. Riverside Plaza
Suite 1500
Chicago, IL 60606
Tel: 800-572-1717
Fax: 520-529-5300

Neuropathy Association
110 West 40th Street
Suite 1804
New York, NY 10018
Tel: 888-PN-FACTS (888-763-2287)
Fax: 212-692-0668

Hereditary Neuropathy Foundation, Inc
432 Park Avenue South
4th Floor
New York, NY 10128
Tel: 855-HELPCMT (435-7268) 212-722-8396

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Prepared by:
Office of Communications and Public Liaison
National Institute of Neurological Disorders and Stroke
National Institutes of Health
Bethesda, MD 20892

NINDS health-related material is provided for information purposes only and does not necessarily represent endorsement by or an official position of the National Institute of Neurological Disorders and Stroke or any other Federal agency. Advice on the treatment or care of an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient's medical history.

All NINDS-prepared information is in the public domain and may be freely copied. Credit to the NINDS or the NIH is appreciated.

Last Modified July 17, 2015