URL of this page: http://www.nlm.nih.gov/medlineplus/ency/article/000727.htm
Alternative names
Progressive neuropathic (peroneal) muscular atrophy; Hereditary peroneal nerve dysfunction; Neuropathy - peroneal (hereditary); Hereditary motor and sensory neuropathyDefinition
Charcot-Marie-Tooth disease is a group of disorders that affect the peripheral nerves, the nerves running from outside the brain and spine.
Causes, incidence, and risk factors
Charcot-Marie-Tooth is one of the most common inherited nerve-related disorders. Defects in at least 14 genes cause different forms of this disease.
The disease involves damage to the covering (myelin sheath) around nerve fibers. In some, the disease causes destruction of the myelin sheath. In others, the central (axon) portion of the nerve cell wears away.
Nerves that stimulate movement (the motor nerves) are most severely affected. The nerves in the legs are affected first and most severely.
Symptoms
Symptoms usually begin between mid-childhood and early adulthood. They may include:
Later, similar symptoms may appear in the arms and hands, which may include a claw-like hand deformity.
Signs and tests
A physical exam may show thickened nerve bundles under the skin of the legs. The stretch reflexes in the legs are absent. There is loss of muscle control and atrophy in the foot or leg. Lifting up the foot and toe-out movements will be difficult.
A muscle biopsy or nerve biopsy may confirm the diagnosis. Nerve conduction tests are often done to tell the difference between different forms of the disorder.
Genetic testing is available for most forms of the disease.
Treatment
There is no known cure. Orthopedic surgery or equipment (such as braces or orthopedic shoes) may make it easier to walk.
Physical and occupational therapy may help maintain muscle strength and improve independent functioning.
Expectations (prognosis)
Charcot-Marie-Tooth disease slowly gets worse. Some parts of the body may become numb, and pain can range from mild to severe. Eventually the disease may cause disability. It is not life threatening.
Complications
Calling your health care provider
Call for an appointment with your health care provider if there is persistent weakness or decreased sensation in the feet or legs.
Prevention
Genetic counseling and testing is advised if there is a strong family history of the disorder.
Update Date: 7/10/2007 Updated by: A.D.A.M. Editorial Team: Greg Juhn, M.T.P.W., David R. Eltz, Kelli A. Stacy. Previously reviewed by Brian Kirmse, MD, Mount Sinai School of Medicine, Department of Human Genetics, New York, NY. Review provided by VeriMed Healthcare Network (5/16/2007).