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         Charcot-marie-tooth Disease:     more books (25)
  1. 21st Century Ultimate Medical Guide to Charcot-Marie-Tooth (CMT) Disease - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-04-04
  2. CHARCOT-MARIE-TOOTH DISEASE by Unknown, 1000
  3. CHARCOT-MARIE-TOOTH DISEASE:A PRACTICAL GUIDE by Unknown, 2000
  4. The Official Patient's Sourcebook on Charcot-Marie-Tooth Disorder: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09
  5. Charcot-Marie-Tooth disorder: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Deepti, MS, CGC Babu, 2005
  6. The Bournemouth questionnaire as an outcome measure in the rehabilitation of a person suffering with mechanical neck and arm pain and concurrent Charcot-Marie-Tooth ... of the Canadian Chiropractic Association by Paul Rankin, 2006-07-01
  7. Charcot-Marie-Tooth: A Guide for Patients and Families (American Academy of Neurology): A Guide for Patients and Families (American Academy of Neurology) by Michael E. Shy, 2007-06-30
  8. Neuromuscular diseases: An entry from Thomson Gale's <i>Gale Encyclopedia of Science, 3rd ed.</i> by Joseph D. Wassersug, 2004
  9. Jean Martin Charcot: An entry from Gale's <i>Science and Its Times</i> by Lois N. Magner, 2000
  10. Genetics in your practice: deciding on genome sequencing.(GENETIC MEDICINE): An article from: Internal Medicine News by Michael F. Murray, 2010-05-01

21. Charcot-Marie-Tooth Disease / Family Village Library
CharcotMarie Tooth Disease (CMT) is the most common neuromuscular disease in the world. It is sometimes referred to as Hereditary Motor and Sensory
http://www.familyvillage.wisc.edu/lib_cmtd.htm
Charcot-Marie-Tooth Disease
Synonym: Peroneal Muscular Atrophy, Hereditary Motor and Sensory Neuropathy
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Charcot-Marie-Tooth Association
2700 Chestnut Street
Chester, PA 19013-4867
1-800-606-CMTA (phone)
1-610-499-9267 (fax)
E-mail: CMTAssoc@aol.com
Web: http://www.charcot-marie-tooth.org/ Works to educate, fund research, and promote public awareness of CMT, the most commonly inherited peripheral neuropathy.
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  • CMT-Support Charcot-Marie Tooth Disease (CMT) is the most common neuromuscular disease in the world. It is sometimes referred to as "Hereditary Motor and Sensory Neuropathy" or HMSN. About one in 2500 people or over 2,000,000 people now have one of the many types of CMT. This group is for sharing feelings as well as life's ups and downs, learning, and mutual support for people with CMT, their friends, families, medical professionals, and anyone that wants to learn about CMT.
  • CMT US CMT US shares resources, positive living strategies, practical suggestions, and new treatment paradigms for Charcot Marie Tooth Disease(CMT), also known as Hereditary Motor and Sensory Neuropathy.

22. Charcot-Marie-Tooth Disease - Podiatrychannel
CharcotMarie-Tooth (CMT) is an inherited, degenerative disease that causes muscle weakness and atrophy of the hand, forearm, leg, and foot.
http://www.podiatrychannel.com/charcot/
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CT Scan MRI Scan RESOURCES DPMLocator Anatomy Clinical Trials Glossary ... What Is a Podiatrist? Videos FOR DOCTORS ONLY Website Services Get Listed in DPMLocator ABOUT US Healthcommunities.com Testimonials Link to podiatrychannel Overview Charcot-Marie-Tooth (CMT) disease, also known as hereditary motor and sensory neuropathy (HMSN), is an inherited, degenerative nerve disorder that causes muscle weakness and atrophy in the feet, legs, hands, and forearms. It is characterized by progressive loss of use and sensation in the limbs. Charcot, Marie, and Tooth are the names of the physicians who identified the disease and described its symptoms. It is not the same as Charcot's foot disease , a neuropathic joint disease that is a common complication of diabetes mellitus.

23. Genome.gov | Learning About Charcot-Marie-Tooth Disease
What do we know about charcotmarie-tooth disease? charcot-marie-tooth disease (CMT) is an inherited neurological disease characterized by a slowly
http://www.genome.gov/11009201
triggerParms["cpp_5"] = "Referer:"+ cppUrlPatch (""); // Optional Home About NHGRI Newsroom Staff ... Specific Genetic Disorders Learning About Charcot-Marie-Tooth Disease
Learning About Charcot-Marie-Tooth Disease
What do we know about Charcot-Marie-Tooth disease? Is there a gene implicated in Charcot-Marie-Tooth? NHGRI Clinical Research on Charcot-Marie-Tooth Additional Resources for Charcot-Marie-Tooth Disease
What do we know about Charcot-Marie-Tooth disease?
Charcot-Marie-Tooth disease (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 muscle cramping, loss of some normal reflexes, occasional partial sight and/or hearing loss, and, in some individuals, scoliosis (curvature of the spine). People with CMT disease usually begin to experience symptoms in adolescence or early adulthood. There is no cure for the disease, but there are treatment options, including physical therapy and bracing. Life expectancy is usually normal.

24. CHARCOT MARIE TOOTH
charcotmarie-tooth disease is a hereditary disorder marked by slowly progressive In both types of charcot-marie-tooth disease, there is normal life
http://www.mda.org.au/specific/mdacmt.html
FACT SHEET CHARCOT - MARIE - TOOTH DISEASE
What is Chacot-Marie-Tooth disease?
Charcot-Marie-Tooth disease is a hereditary disorder marked by slowly progressive muscle weakness in the feet, lower legs, hands and forearms, and a mild loss of sensation in limbs, fingers, and toes. The weakness results from the degeneration of nerves that stimulate muscle rather than from a degenerative process in the muscle tissue itself. The disorder, named for three physicians who first identified it in 1886, is also known as peroneal muscular atrophy because if primarily affects the peroneal muscles. which are located in the lower leg. There are now thought to be at least two types of the disease - hypertrophic and neuronal - that differ to some degree in severity.
How disabling is the disease? In both types of Charcot-Marie-Tooth disease, there is normal life expectancy, limited disability, and very slow progression of the disease. Some patients, however, experience rapid progression and severe disability.
What are the early symptoms?

25. BBC - Health - Conditions - Charcot-Marie-Tooth Disease
Discover the causes, symptoms and treatments of this neurological disorder.
http://www.bbc.co.uk/health/conditions/charcotmarietooth1.shtml
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Charcot-Marie-Tooth disease
Dr Trisha Macnair Discover the symptoms and treatments of this inherited neurological disorder, plus links to some useful support groups in the UK and abroad.
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What is it? Symptoms Who's affected? Diagnosis and treatment
What is it?
Charcot-Marie-Tooth disease - also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy - is the name given to a group of conditions where the nerves to the muscles, particularly in the lower leg and hands, don't work properly. The part of the nerves carrying sensory signals back towards the brain may also be affected, leading to altered sensation in the affected areas. There are at least four different types of HMSN, which were originally classified on the basis of electrical tests of nerve conduction. But as genetic causes for these different conditions are discovered, so HMSN conditions are being reclassified into a wider group of disorders. Other features include high arched feet in many cases and, in some less common types, deafness, problems with vision, paralysis of the vocal cords and breathing difficulties.

26. Charcot-Marie-Tooth Disease - MayoClinic.com
charcotmarie-tooth disease includes a group of disorders that affect the peripheral nerves, causing muscle weakness and loss of muscle bulk.
http://www.mayoclinic.com/invoke.cfm?id=DS00557

27. Charcot-Marie-Tooth Disease (www.whonamedit.com)
charcotmarie-tooth disease A syndrome characterized by slowly progressive wasting and weakness of distal muscle of the arms and feet, the commonest
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Charcot-Marie-Tooth disease Also known as: Charcot-Marie syndrome Charcot-Marie-Tooth-Hoffmann disease (Johann Hoffmann) Charcot-Marie-Tooth-Hoffmann syndrome (Johann Hoffmann) Tooth muscular atrophy Tooth’s syndrome Synonyms: Atrophia musculorum progressiva neurotica sive neuralis, hereditary motor and sensory neuropathy I (HMSN I), neuropathic muscular atrophy, peroneal muscle atrophy. Associated persons: Jean-Martin Charcot Johann Hoffmann Pierre Marie Howard Henry Tooth Description: Charcot-Marie-Tooth disease, the so-called neural or spinal form of muscular atrophy, is the commonest disease within a group of conditions called Hereditary Motor and Sensory Neuropathies (HMSN).

28. Charcot-Marie-Tooth Disease (CMT)
Penn State Hershey Medical Center provides world class care and services to patients.
http://www.hmc.psu.edu/healthinfo/c/cmt.htm

29. Charcot-Marie-Tooth Disease (hereditary)
charcotmarie-tooth disease defines a group of inherited, slowly progressive disorders that result from progressive damage to nerves.
http://www.healthcentral.com/ency/408/000727.html
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Definition: Charcot-Marie-Tooth disease defines a group of inherited, slowly progressive disorders that result from progressive damage to nerves. Symptoms include

30. Charcot-Marie-Tooth Disease- Health Encyclopedia And Reference
charcotmarie-tooth disease Symptoms, Treatments and Medications.
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31. Charcot-Marie-Tooth Disease
CHC Wausau Hospital s Medical Library and Patient Education Center provides research services and healthcare information to physicians,
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Charcot-Marie-Tooth disease
Definition
Charcot-Marie-Tooth disease (CMT) is the name for a group of inherited disorders of nerve conduction causing weakness and mild loss of sensation in the limbs. Description
CMT affects the peripheral nerves, those groups of nerve cells carrying information to and from the spinal cord. CMT decreases the ability of these nerves to carry motor commands to muscles, especially those furthest from the spinal cord in the feet and hands. As a result, these muscles are weakened. CMT also causes mild sensory loss. CMT is named for the three neurologists who first described it, and does not involve the teeth in any way. It is also known as hereditary motor and sensory neuropathy, and is also sometimes called peroneal muscular atrophy, referring to the muscles in the leg affected early on in the disease.
Causes
The symptoms grouped together under the name CMT can be caused by any of at least six different genetic defects. Most of the defects, identified as of early 1998, affect myelin, the coating that insulates nerve cells to promote efficient conduction. Myelin defects cause either a reduction in nerve conduction velocities, or a diminished nerve signal. CMT is currently subdivided into type 1A, type 1B, type 2, and type X, based on the particular genetic defect involved. All but type X exhibit the inheritance pattern known as autosomal dominant. In this pattern, only one defective gene copy is needed to develop the disease, which may be inherited from either parent (who will also have the disease). A person with CMT of this type has a 50% chance of passing the gene along to each offspring. CMT type X is inherited as an X-linked trait, meaning the gene is carried on the X chromosome. Women carry two X chromosomes, while men carry only one. Without a "backup" copy of the normal gene, a man with the CMT type X gene is more likely to be seriously affected than is a woman. Expression of the gene does occur in women to a lesser extent, leading to disease of variable severity. Affected men may pass the gene on to their daughters, but not to their sons.

32. Encyclopaedia Topic : Charcot-Marie-Tooth Disease, Section : Introduction
CharcotMarie-Tooth (CMT) disease is named after the three neurologists who first Dejerine-Sottas Disease is also very similar to Charcot-Marie-Tooth
http://www.nhsdirect.nhs.uk/en.asp?TopicID=622

33. Encyclopaedia Topic : Charcot-Marie-Tooth Disease, Section : Symptoms
NHS Direct Online Health Encyclopaedia. charcotmarie-tooth disease The disease weakens the muscles and people with CMT will usually experience some
http://www.nhsdirect.nhs.uk/en.asp?TopicID=622&AreaID=4097&LinkID=3172

34. Charcot-Marie-Tooth Disease
Feature article describes the charcotmarie-tooth diseases, their diagnoses, and treatments.
http://rarediseases.about.com/cs/cmt/a/032001.htm
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Elsewhere on the Web Charcot-Marie-Tooth Association (U.S.)

35. Gene Associated With Charcot-Marie-Tooth Disease Identified
Several years ago researchers identified a region on chromosome 1 as having the gene responsible for charcotmarie-tooth disease (CMT), a degenerative nerve
http://rarediseases.about.com/b/a/080108.htm
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Gene associated with Charcot-Marie-Tooth disease identified
Rare/Orphan Diseases Blog Main
April 19, 2004
Gene associated with Charcot-Marie-Tooth disease identified
Several years ago researchers identified a region on chromosome 1 as having the gene responsible for Charcot-Marie-Tooth disease (CMT), a degenerative nerve disorder, but did not know the exact gene involved. Researchers at the Duke Center for Human Genetics have now identified a gene, known as mitofusin 2, that is associated with CMT type 2A. The gene is critical to the development of mitochondria, the structures in a cell that produce energy. The research was reported in the April 4, 2004, issue of Nature Genetics
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36. Healthfinder® - Charcot-Marie-Tooth Disease
Carefully selected government and nonprofit health information on charcotmarie-tooth disease.
http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=151

37. Healthfinder® — Charcot-Marie-Tooth Disease Fact Sheet
This is a fact sheet about charcotmarie-tooth disease. CMT, also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy,
http://www.healthfinder.gov/Scripts/ShowDocDetail.asp?doc=7202&lang=1

38. Types Of Peripheral Neuropathy - Hereditary - Charcot-Marie-Tooth Disease (CMT)
charcotmarie-tooth disease (CMT) is a broad term used to describe a group of inherited neurological disorders characterized by a slowly progressive
http://millercenter.uchicago.edu/learnaboutpn/typesofpn/hereditary/charcotmariet
What is Peripheral Neuropathy Peripheral Neuropathy Symptoms Types of Peripheral Neuropathy Evaluation and Tests ... Frequently Asked Questions
Types of Peripheral Neuropathy - Hereditary
Idiopathic Pre-diabetic/Diabetic Hereditary Toxic/Secondary to Drugs ... Other Types of PN Charcot-Marie-Tooth Disease (CMT) Charcot-Marie-Tooth disease (CMT) is a broad term used to describe a group of inherited neurological disorders 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. Three French doctors, Jean-Marie Charcot, Pierre Marie, and Howard Henry Tooth, discovered CMT in 1886. Although CMT is one of the most common inherited neuromuscular disorders, it is often misdiagnosed. The number of people in the United States that have CMT is currently estimated to be 125,000. The symptoms of CMT depend on which form of the disease is inherited, but generally start between mid-childhood and early adulthood. The first signs are usually foot abnormalities, such as an unusually high arch or flexed ("hammer") toes. People with CMT often trip on curbs. Sprained ankles and fractures of the ankles and lower legs are not uncommon. As the disease progresses, muscle weakness and wasting leads to difficulties with walking, running and balance. If the hands are affected, daily activities such as turning doorknobs, fastening buttons, or writing can become difficult. The disease is slowly progressive and, although many patients need to wear a brace to prevent their feet from dragging, the leg and foot problems are rarely disabling enough to require a wheelchair. CMT is not a fatal disease and the disorder does not affect normal life expectancy.

39. Charcot-Marie-Tooth Disease
charcotmarie-tooth disease. From MayoClinic.com Special to CNN.com. Overview. Charcot-Marie-Tooth (CMT) disease broadly includes a group of progressive
http://www.cnn.com/HEALTH/library/DS/00557.html
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    Overview Charcot-Marie-Tooth (CMT) disease broadly includes a group of progressive hereditary disorders that cause nerve damage (neuropathy). The damage in CMT occurs to your peripheral nerves or to the insulation covering your nerves (myelin sheath). The peripheral nerves are those outside of your central nervous system (brain and spinal cord). CMT most often affects the legs, feet and hands. It generally results in muscle weakness and loss of muscle bulk. In some cases, it may cause a mild loss of sensation. Named after the three physicians who first identified the disorder in 1886, CMT is a common inherited neurological disorder. It affects approximately 150,000 people in the United States and occurs in all races and ethnic groups. CMT most often is discovered between midchildhood and age 30, but can develop at any age.

40. Information On Charcot Marie Tooth Disease And Brain Disorders At MedicineNet.co
Learn about charcotmarie-tooth disease, an inherited neurological disorder.
http://www.medicinenet.com/charcot-marie-tooth-disease/article.htm
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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. The disease is named for the three physicians who first identified it in 1886 - Jean-Martin Charcot and Pierre Marie in Paris, France, and Howard Henry Tooth in Cambridge, England. CMT, also known as hereditary motor and sensory neuropathy (HMSN) or peroneal muscular atrophy, comprises a group of disorders that affect peripheral nerves. The peripheral nerves lie outside the brain and spinal cord and supply the muscles and sensory organs in the limbs. Disorders that affect the peripheral nerves are called peripheral neuropathies. What are the symptoms of Charcot-Marie-Tooth-disease?

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