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AR-CMT2; Charcot-Marie-Tooth disease, type 1; Charcot-Marie-Tooth disease, type 2; Charcot-Marie-Tooth disease, type 4; ... |
Neuropathy - Hereditary | |
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Charcot-Marie-Tooth disorder (CMT) is an inherited neurological disease characterized by a slowly progressive degeneration of the muscles in the foot, lower leg, hand, and forearm, and a mild loss of sensation in the limbs, fingers, and toes. The first sign of CMT is generally a high arched foot or gait disturbances. Other symptoms of the disorder may include foot bone abnormalities such as high arches and hammer toes, problems with hand function and balance, occasional lower leg and forearm mus... 
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A problem in peripheral nerve function (any part of the nervous system except the brain and spinal cord) that causes pain, numbness, tingling, swelling, and muscle weakness in various parts of the body. Neuropathies may be caused by physical injury, infection, toxic substances, disease (e.g., cancer, diabetes, kidney failure, or malnutrition), or drugs such as anticancer drugs. Also called peripheral neuropathy.
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Charcot-Marie-Tooth Disease as related to Neuropathy
- Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth disease (CMT) is a progressive motor and sensory neuropathy (nerve disorder) characterized by weakness and atrophy, primarily in the leg muscles. It also known ...
- Charcot-Marie-Tooth Neuropathy Type 2 -- GeneReviews -- NCBI ...
CMT2; Charcot-Marie-Tooth Disease, Axonal Type; HMSN2; Hereditary Motor and Sensory Neuropathy 2. Includes: CMT2A1, CM2A2, CMT2B, CMT2B1, CMT2B2, CMT2C, CMT2D, CMT2E/1F, CMT2F ...
- Charcot-Marie-Tooth Neuropathy Type 1 -- GeneReviews -- NCBI Bookshelf
Summary. Disease characteristics. Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a demyelinating peripheral neuropathy characterized by distal muscle weakness and atrophy, sensory ...
- Hereditary Neuropathy Foundation
An information web site for the Charcot-Marie-Tooth disease. ... Plans are only good intentions unless they immediately degenerate into hard work.
- Charcot-Marie-Tooth Disease / Family Village Library
Charcot-Marie-Tooth Disease Synonym: Peroneal Muscular Atrophy, Hereditary Motor and Sensory Neuropathy. Who to Contact Where to Go to Chat with Others
- Charcot-Marie-Tooth disease - Wikipedia, the free encyclopedia
Charcot-Marie-Tooth disease ( CMT ), known also as Hereditary Motor and Sensory Neuropathy ( HMSN ) or Peroneal Muscular Atrophy , is a heterogeneous inherited disorder of nerves that is characterized by loss of muscle tissue and touch sensation, predominantly in the feet and legs but also in the hands and arms in the advanced stages of disease.
Description · Symptoms · Diagnosis · Types of the disease · Genetic testing
- Charcot-Marie-Tooth Association - CMTA
Charcot-Marie-Tooth Association 2700 Chestnut Street, Chester, PA 19013 ... should not be used to diagnose, treat, cure or prevent any disease or ...
- Charcot-Marie-Tooth Disease (CMT) - Welcome to MDA | Muscular ...
Last updated 7/07: Charcot-Marie-Tooth Disease (CMT) (Also known as Hereditary Motor and Sensory Neuropathy ...
- Charcot-Marie-Tooth disease (hereditary)
From our partner site on chronic pain , ChronicPainConnection.com. Charcot-Marie-Tooth diseases involve damage to nerves (neuropathy), usually from loss of the electrical ...
- Charcot-Marie-Tooth Disease: St. Joseph Mercy, Ann Arbor Michigan
Charcot-Marie-Tooth Disease, St. Joseph ... Hereditary Neuropathy Foundation. International network. Founded 2001. Sharing and caring for those with Charcot-Marie-Tooth disease, and ...
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