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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 (www.whonamedit.com)
If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here see a doctor. charcotmarie-tooth disease
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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). A syndrome characterized by slowly progressive wasting and weakness of distal muscle of the arms and feet, caused by degeneration of the peripheral nerves, nerve roots, and even the spinal cord, with loss of reflexes, loss of cutaneous sensations and develeopment of foot drop. Optic atrophy is sometimes present.

22. CHARCOT-MARIE-TOOTH DISEASE : Contact A Family - For Families With Disabled Chil
printer friendly, charcotmarie-tooth disease, charcot-marie-tooth disease CMT Peroneal Muscular Atrophy Hereditary Motor and Sensory Neuropathy.
http://www.cafamily.org.uk/Direct/c27.html
printer friendly CHARCOT-MARIE-TOOTH DISEASE home more about us in your area conditions information ... how you can help search this site Did you find this page
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yes no Charcot-Marie-Tooth disease: CMT: Peroneal Muscular Atrophy: Hereditary Motor and Sensory Neuropathy This is a genetic disorder characterised by slowly progressive muscular weakness. Onset is in the lower limbs first causing weakness around the ankles and, often, an abnormality in the shape of the feet (high in-step.) After many years, weakness may develop in the hands and spread upwards in the lower limbs to affect the knees and thighs. Mild loss of sensation may be present in the feet and hands. The onset of the condition may be from childhood to late middle or old age. Inheritance patterns
  • Autosomal dominant is the most common pattern of inheritance.
  • Autosomal recessive (least common)
  • X-linked passed to both sons and daughters. However, affected sons will usually display more severe symptoms.
Prenatal diagnosis
In families who have Type 1a prenatal diagnosis is now becoming available but is rarely requested.

23. Orthoseek | Orthopedic Topics | Charcot-Marie-Tooth Disease
charcotmarie-tooth disease or Peroneal Muscular Atrophy is the commonest disease within a group of conditions called Hereditary Motor and Sensory Neuropathies
http://www.orthoseek.com/articles/cmtdisease.html
Charcot-Marie-Tooth Disease
What is it? Charcot-Marie-Tooth disease or Peroneal Muscular Atrophy is the commonest disease within a group of conditions called Hereditary Motor and Sensory Neuropathies (HMSN) . This group of diseases are caused by degeneration of the peripheral nerves, nerve roots, and even the spinal cord. Charcot-Marie-Tooth disease is also known as HMSN Type I, and is the most common disease in the group. The nerves that supply the small muscles of the feet are affected, causing weakness and deformity in the feet. There is also loss of position and vibration sense to the feet. Much later, the small muscles of the hands are also affected. What causes it? The disease is hereditary, and is inherited as an autosomal dominant trait. What are the symptoms? The affected child presents with high arches in his feet, as well clumsiness and pain in his feet and legs. Due to muscle imbalance in the feet, the child may develop a dropfoot , as well as a cavus foot , where the arch of the foot is very pronounced and fixed. Later, if the small muscles of the hands are also affected, he may develop clawing of the fingers. The affected child has normal intelligence, and a normal life span.

24. Charcot-Marie-Tooth Disease
charcotmarie-tooth disease. I am What is it? charcot-marie-tooth disease refers to a group of disorders with similar symptoms. In CMT
http://rarediseases.about.com/cs/cmt/a/032001.htm
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25. Gene Associated With Charcot-Marie-Tooth Disease Identified
Gene associated with charcotmarie-tooth disease identified. Rare/Orphan Diseases Blog. « Kartagener Syndrome Main Wolf-Hirschhorn Syndrome ».
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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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26. Charcot-Marie-Tooth Disease - Information / Diagnosis / Treatment / Prevention
home neurological disorders peripheral nervous system charcotmarie-tooth disease charcot-marie-tooth disease. Information
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Related Topics: Genetic Disorders Rare Disorders Medical Definition: University of Newcastle-upon-Tyne Medical Dictionary: "Charcot-Marie-Tooth disease" Health News: Search millions of published articles for news on Charcot-Marie-Tooth Disease Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: Charcot-Marie-Tooth Association Includes information about the organization, its goals, research, news and further resources. Also offers suggestions on ways to help. Charcot-Marie-Tooth Disorder Information page compiled by National Institute of Neurological Disorders and Stroke.

27. Charcot-Marie-Tooth Disease (CMT)
charcotmarie-tooth disease (CMT). What is it? charcot-marie-tooth disease (CMT) is an inherited disorder that affects the nerves
http://www.hmc.psu.edu/healthinfo/c/cmt.htm

28. Charcot-Marie-Tooth Disease - Causes, Symptoms & Treatment
charcotmarie-tooth disease Fact Book. Table of Contents What is charcot-marie-tooth disease? charcot-marie-tooth disease (CMT) is
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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-Marie-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. Back to Top Click Here for the Latest News on CMT Back to Top
What are the symptoms of Charcot-Marie-Tooth disease?

29. Encyclopaedia Topic : Charcot-Marie-Tooth Disease, Section : Introduction
charcotmarie-tooth disease. Search. Help. Dejerine-Sottas Disease is also very similar to charcot-marie-tooth disease and is sometimes referred as CMT3.
http://www.nhsdirect.nhs.uk/en.asp?TopicID=622

30. Encyclopaedia Topic : Charcot-Marie-Tooth Disease, Section : Causes
NHS Direct Online Health Encyclopaedia. charcotmarie-tooth disease. Search. Help. Sections for this topic
http://www.nhsdirect.nhs.uk/en.asp?TopicID=622&AreaID=4098&LinkID=3173

31. Types Of Peripheral Neuropathy - Hereditary - Charcot-Marie-Tooth Disease (CMT)
charcotmarie-tooth disease (CMT). charcot-marie-tooth disease (CMT) is a broad term used to describe a group of inherited neurological
http://millercenter.uchicago.edu/learnaboutpn/typesofpn/hereditary/charcotmariet
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.

32. Charcot-Marie-Tooth Disease - Medical Dictionary Definitions Of Popular Medical
MedicineNet Home MedTerms medical dictionary AZ List charcotmarie-tooth disease. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=13609

33. Charcot-Marie-Tooth-Disease -- ECureMe.com
charcotmarie-tooth disease, more about charcot-marie-tooth disease, charcot-marie-tooth disease causes destruction of the peripheral nerves.
http://www.ecureme.com/emyhealth/data/Charcot-Marie-Tooth-Disease.asp
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Hereditary sensorimotor neuropathies
  • Charcot-Marie-Tooth disease is a type of peripheral Neuropathy , characterized by a slowly progressive weakness and wasting of the muscles in the upper and lower extremities.

34. National Human Genome Research Institute - Learning About Charcot-Marie-Tooth Di
Specific Genetic Disorders Learning About charcotmarie-tooth disease, Learning About charcot-marie-tooth disease.
http://www.genome.gov/11009201

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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.

35. Healthfinder® - Charcot-Marie-Tooth Disease
home health library all topics C charcotmarie-tooth disease. displaying 1–1 of 1 document see categories and related topics,
http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=151

36. Healthfinder® — CMT International (Charcot-Marie-Tooth Disease/Peroneal Muscul
CMT International (charcotmarie-tooth disease/Peroneal Muscular Atrophy International Association, Inc.). organization URL(s). cmtint@vaxxine.com.
http://www.healthfinder.gov/orgs/HR2300.htm
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CMT International (Charcot-Marie-Tooth Disease/Peroneal Muscular Atrophy International Association, Inc.)
organization URL(s)
cmtint@vaxxine.com
other contact information
1 Springback Drive
St. Catherines
Ontario, Canada, L2S 2K1 905-687-3630 (Voice)
905-687-8753 (FAX)
description
CMT International, a registered Canadian charitable organization, is concerned with the physical and psychological needs of those with Charcot-Marie-Tooth Disease, also known as Peroneal Muscular Atrophy or heredity motor and sensory neuropathy (HMSN). CMT International sponsors local chapters throughout the United States, Canada, and the United Kingdom. CMT International sends out a 32 page newsletter to members 6 times a year, a video on CMT, and various publications on specific problems. CMT International also funds scholarships through the head office.
print resources
Serial publication: CMT Newsletter, bimonthlymedical and research articles; coping strategies, and member profiles.
related topics
Charcot-Marie-Tooth Disease Neuromuscular Diseases Neuropathy
review date
Wed Apr 15, 1998

37. Charcot-Marie-Tooth Disease Definition Of Charcot-Marie-Tooth Disease. What Is C
charcotmarie-tooth disease. Word Word. Some words with charcot-marie-tooth disease in the definition
http://www.thefreedictionary.com/Charcot-Marie-Tooth disease
Dictionaries: General Computing Medical Legal Encyclopedia
Charcot-Marie-Tooth disease
Word: Word Starts with Ends with Definition Noun Charcot-Marie-Tooth disease - a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant hereditary motor and sensory neuropathy neuropathy - any pathology of the peripheral nerves Legend: Synonyms Related Words Antonyms Some words with "Charcot-Marie-Tooth disease" in the definition: ankylosing spondylitis
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38. HealthCentral - General Encyclopedia - Charcot-Marie-Tooth Disease (hereditary)
General Health Encyclopedia, charcotmarie-tooth disease (hereditary). Treatment There is no known cure for charcot-marie-tooth disease.
http://www.healthcentral.com/mhc/top/000727.cfm
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39. Disease - Charcot-Marie-Tooth Disease (CMT)
2004. Please Rate this Page. charcotmarie-tooth disease (CMT). Disease Name, charcot-marie-tooth disease (CMT). SearchTerm, Hereditary
http://disability.ucdavis.edu/resources/diseases/list/disease.asp?id=5

40. || DukeMedNews || Genetic Testing For Charcot-Marie-Tooth Disease
all dates, Genetic testing for charcotmarie-tooth disease. Back to List,
http://dukemednews.org/news/article.php?id=5152

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