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Charcot-Marie-Tooth disease

Contents of this page:

Illustrations

Central nervous system
Central nervous system

Alternative Names    Return to top

Progressive neuropathic (peroneal) muscular atrophy; Hereditary peroneal nerve dysfunction; Neuropathy - peroneal (hereditary); Hereditary motor and sensory neuropathy

Definition    Return to top

Charcot-Marie-Tooth disease is a group of disorders that affect the peripheral nerves, the nerves running from outside the brain and spine.

Causes    Return to top

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    Return to top

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.

Exams and Tests    Return to top

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    Return to top

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.

Outlook (Prognosis)    Return to top

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.

Possible Complications    Return to top

When to Contact a Medical Professional    Return to top

Call for an appointment with your health care provider if there is persistent weakness or decreased sensation in the feet or legs.

Prevention    Return to top

Genetic counseling and testing is advised if there is a strong family history of the disorder.

Update Date: 12/12/2008

Updated by: A.D.A.M. Editorial Team: David Zieve, MD, MHA, Greg Juhn, MTPW, David R. Eltz. 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).

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