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         Charcot-marie-tooth Disease:     more books (25)
  1. 21st Century Complete Medical Guide to Charcot-Marie-Tooth Disease (CMT), Hereditary Motor and Sensory Neuropathy (HMSN), Peroneal Muscular Atrophy, Authoritative ... for Patients and Physicians (CD-ROM) by PM Medical Health News, 2004-03
  2. Coping with Charcot Marie Tooth Disease (Volume 1) by Diane M Gracely, 2010-06-16
  3. Charcot-Marie-Tooth Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-16
  4. Charcot-Marie-Tooth disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Karen, MS, CGC Krajewski, 2005
  5. Charcot-Marie-Tooth Disease: A Practical Guide. Also Known as Hereditary Motor and Sensory Neuropathy and Peroneal Muscular Atrophy. by (No Author), 2000
  6. Charcot-Marie-Tooth Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  7. Charcot-Marie-Tooth disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Christine Kelly, 2006
  8. Gale Encyclopedia of Medicine: Charcot Marie Tooth disease by CGC Karen M. Krajewski MS, 2002-01-01
  9. CHARCOT-MARIE-TOOTH DISEASE: A PROCTICAL GUIDE.
  10. Charcot-Marie-Tooth disease and multiple malignant melanomas: a case report.(Case study): An article from: Journal of Drugs in Dermatology by Ritu Saini, Stephanie Lehrhoff, et all 2010-02-01
  11. Charcot Marie Tooth Disease: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Karen, MS, CGC Krajewski, 2006
  12. Charcot-Marie-Tooth Disorders (Annals of the New York Academy of Sciences)
  13. 2009 Conquering Charcot-Marie-Tooth (CMT) Disease - The Empowered Patient's Complete Reference - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) by PM Medical Health News, 2009-04-04
  14. Charcot-Marie-Tooth (CMT) Disease Toolkit - Comprehensive Medical Encyclopedia with Treatment Options, Clinical Data, and Practical Information (Two CD-ROM Set) by U.S. Government, 2009-04-04

1. CMTA: Charcot-Marie-Tooth Association
charcotmarie-tooth disease
http://www.charcot-marie-tooth.org/
We are pleased to present your renovated CMTA website. This is truly your site as it is intended to provide you with current useful information about CMT. Click for more info. Swim for the Cure Support Steve O'Donnell Click Here
Enter
Click here to Sign-Up
A Visit to the Wayne State CMT Clinic in Detroit, Michigan

Issues Affecting Children Scoliosis... A Secondary Concern with CMT

Nerve Conduction Velocity Test

Vocational Rehabilitation...
... Help the Cause... Push Rare Disease Legislation
Together, we can educate, fund research, and promote public awareness of CMT as the most common cause of hereditary motor sensory neuropathy.
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When you shop at GreaterGood.com up to 15% of every purchase automatically goes to Charcot-Marie-Tooth Association at no extra cost to you.
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2. Charcot-Marie-Tooth Disease - Neurologychannel
Incidence and Prevalence Approximately 125,000 people in the UnitedStates have charcotmarie-tooth disease. CMT occurs slightly
http://www.neurologychannel.com/charcot/
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Botulinum Toxin Therapy Epidural Injection Trigger Point Injection Vagus Nerve Stimulation RESOURCES Clinical Trials Links Videos ABOUT US Healthcommunities.com Pressroom Testimonial Overview Charcot-Marie-Tooth (CMT) disease is an inherited, degenerative peripheral 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. In CMT, the

3. Charcot-Marie-Tooth Disease (CMT) (aka HMSN Or Peroneal Muscular Atrophy (PMA))
charcotmarie-tooth disease (CMT) (Also known as Hereditary Motor and Sensory Neuropathy(HMSN) or Peroneal Muscular Atrophy (PMA)) Click for Materials En
http://www.mdausa.org/disease/cmt.html
Charcot-Marie-Tooth Disease (CMT)
(Also known as Hereditary Motor and Sensory Neuropathy (HMSN) or Peroneal Muscular Atrophy (PMA))
Click for and MDAchats
Bookmark this page!
It's your source for information and news about CMT and will be updated regularly.
Quick Definition:
Childhood to young adulthood. Weakness and atrophy of muscles of hands and lower legs, with foot deformities and some loss of sensation in feet. Slow but variable progression among individuals. Normal life span. Autosomal dominant, autosomal recessive, X-linked recessive, X-linked dominant.
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Do you need to find MDA in your city? Enter your Zip code here for where to turn for clinics and medical services; support groups; summer camp; local events and volunteer and fund-raising opportunities close to home.
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4. Facts About Rare Muscular Dystrophies
Describes the history and symptoms of CharcotMarie-Tooth, including inheritance patterns and efforts to find a cure for the disorder.
http://www.mdausa.org/publications/fa-cmt.html
Facts About Charcot-Marie-Tooth Disease and Dejerine-Sottas Disease
Charcot-Marie-Tooth Disease and Dejerine-Sottas Disease
Dear Friends
What Is Charcot-Marie-Tooth Disease? What Causes CMT? What Happens to Someone With CMT, and How Is It Treated? ... MDA Is Here to Help You
George J. Donahue Dear Friends: I've lived with Charcot-Marie-Tooth disease This pamphlet has been prepared to give you the basic knowledge about CMT and Dejerine-Sottas disease that you'll need, in order to help you prepare for changes that may occur in your future. You'll learn that CMT is usually quite slow in progression and that, while it presents challenges in daily life, there are many techniques and devices to help you adapt to those challenges. You'll read that many different genetic causes of CMT have been found, and cases vary greatly. But CMT is almost never life-threatening, and it seldom affects the heart and breathing functions. Another important extended family in my life is the Muscular Dystrophy Association, which offers a great program of services, leads the world in CMT research and keeps us well informed about the disease. See " MDA Is Here to Help You ," for details of the Association's program.

5. Charcot-Marie-Tooth Disease
of CM-T "How I AM" (hope this helps you understand) A Poem written about neuropathy (mine is CMT) by Janice De Vore-Robinson "Just The Way I Am" by Janice De Vore-Robinson......A
http://www.geocities.com/parrotsville/C-M-T.html
Charcot-Marie-Tooth
A Description of C-M-T
"How I AM" (hope this helps you understand) A Poem written about neuropathy (mine is CMT) by Janice De Vore-Robinson
"Just The Way I Am"

by Janice De Vore-Robinson
Doing time for no known crime Has been difficult for me It's hard to live with chronic pain That others cannot see
The thief that robbed my body Stole my strength and left me pain I do my very best to cope I struggle to stay sane
I miss our get-togethers I miss shopping at the mall It hurts me to be left behind It's not my choice at all
I long for how it used to be When I could join right in To do the fun and simple things With family and friends
You seldom call or visit You're tired of it, I guess Of always asking, "Come along" And never hearing, "Yes"
I ache to be with all of you I wish I could explain How doing 'normal' things in life Can cause me so much pain I'm trapped inside this body With pain that has no end I grieve for all the things I've lost I'd like them back again When I decline to join you Please try to understand It's not that I don't want to It's just the way I am by Janice De Vore-Robinson Don't Call Me Disabled I have C-M-T 1 A Jazzy Power Chairs How Stella Got her Jazzy Back I got my Jazzy 1120 Power Chair 7/10/00 C-M-T Association MDA~Charcot-Marie-Tooth Disease (CMT) (Also known as Hereditary Motor and Sensory Neuropathy (HMSN) or Peroneal Muscular Atrophy (PMA)) ...A Guide to Related Materials on MDA's Web Site

6. CMTnet: Charcot-Marie-Tooth Disorders Information Exchange
Information on research and treatment of CMT. Link to practitioner information and details of therapy and DNA testing. CMTnet is a repository of information for research and treatment of CharcotMarie-Tooth (CMT).
http://www.ultranet.com/~smith/CMTnet.html
The purpose
CMTnet is a repository of information for research and treatment of Charcot-Marie-Tooth (CMT). CMT is a hereditary progressive neuromuscular disorder that primarily effects the feet, legs and hands. CMTnet is intended to provide information for both the medical and non-medical communities. Last updated: 1/12/2000. Enter CMTnet

7. MEDLINEplus: Charcot-Marie-Tooth Disease
Topics. charcotmarie-tooth disease. Contents Organizations. Search MEDLINEfor recent research articles on • charcot-marie-tooth disease. You
http://www.nlm.nih.gov/medlineplus/charcotmarietoothdisease.html
Skip navigation
Other health topics: A B C D ... List of All Topics
Charcot-Marie-Tooth Disease
Contents of this page:
From the NIH

General/Overviews

Coping

Diagnosis/Symptoms
...
Organizations

Search MEDLINE for recent research articles on
Charcot-Marie-Tooth Disease
You may also be interested in these MEDLINEplus related pages:
Degenerative Nerve Diseases

Muscle Disorders
Brain and Nervous System Genetics/Birth Defects From the National Institutes of Health
  • Charcot-Marie-Tooth Disease (National Institute of Neurological Disorders and Stroke) Charcot-Marie-Tooth Disorder (National Institute of Neurological Disorders and Stroke)
  • General/Overviews
  • Facts About Charcot-Marie-Tooth Disease (CMT) (Muscular Dystrophy Association) Also available in: Spanish Facts About Charcot-Marie-Tooth Disease (CMT): Questions and Answers (Muscular Dystrophy Association)
  • Clinical Trials
  • Clinical Trials: Identification of Gene Mutations in Families with Charcot-Marie-Tooth and Deafness (Muscular Dystrophy Association)
  • Coping
  • Bracing Experiences: Correct Braces Can Improve Mobility, Life (Muscular Dystrophy Association)
  • Diagnosis/Symptoms
  • Creatine Kinase Test (Muscular Dystrophy Association) Electromyography and Nerve Conduction Velocities (Muscular Dystrophy Association) Muscle Biopsies (Muscular Dystrophy Association)
  • Research
  • Facts About Charcot-Marie-Tooth Disease (CMT): MDA's Search For a Treatment or Cure (Muscular Dystrophy Association) From Clear-Cut Endings to Complex Beginnings: Researchers Probe the Origins of Charcot-Marie-Tooth Disease (Muscular Dystrophy Association)
  • 8. MEDLINEplus Medical Encyclopedia: Charcot-Marie-Tooth Disease (hereditary)
    charcotmarie-tooth disease (hereditary). Treatment Return to top Thereis no known cure for charcot-marie-tooth disease. Treatment
    http://www.nlm.nih.gov/medlineplus/ency/article/000727.htm
    Skip navigation
    Medical Encyclopedia
    Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z
    Charcot-Marie-Tooth disease (hereditary)
    Contents of this page:
    Illustrations
    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 defines a group of slowly progressive, inherited disorders that result from progressive damage to nerves. In addition to loss of sensation, there is wasting of muscle tissue in the feet and legs, then hands and arms. Causes, incidence, and risk factors Return to top Charcot-Marie-Tooth diseases involve damage to nerves (neuropathy), usually from demyelination or loss of the electrical insulation around nerve fibers. All nerves are affected, but motor nerves are disproportionately so. The nerves in the legs are affected first and most severely. Symptoms usually begin between mid-childhood and early adulthood. The disorder is inherited, with autosomal dominant and recessive as well as X-linked recessive inheritance patterns. At least four genes have been discovered to be the cause of this group of diseases.

    9. Charcot-Marie-Tooth Syndrome
    charcotmarie-tooth disease (CMT) disease is named after its three discoverers,who first noted the disease around the turn of the century.
    http://www.ncbi.nlm.nih.gov/disease/Charcot.html
    This Genes and Disease page has been moved to:
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    Genome View
    on chromosome 17
    Databases
    PubMed

    the literature
    LocusLink

    collection of gene-related information
    OMIM

    catalog of human genes and disorders Information Charcot-Marie-Tooth Association patient support, education and research Charcot-Marie-Tooth International run by and for people who have CMT disease GeneClinics a medical genetics resource CHARCOT-MARIE-TOOTH disease (CMT) disease is named after its three discoverers, who first noted the disease around the turn of the century. It is the most common inherited peripheral neuropathy in the world, 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. Full expression of CMT's clinical symptoms generally occurs by age 30. CMT is not a fatal disease, however, and the disorder does not affect normal life expectancy. CMT is a genetically heterogeneous disorder, in which mutations in different genes can produce the same clinical symptoms. In CMT, there are not only different genes but different patterns of inheritance. One of the most common forms of CMT is Type 1A. The gene for Type 1A CMT maps to chromosome 17 and is thought to code for a protein (PMP22) involved in coating peripheral nerves with myelin, a fatty sheath that is important for their conductance. Other types of CMT include Type 1B, autosomal-recessive and X-linked.

    10. Welcome To CMT United Kingdom
    Support group for people with this disease and general information about it.Category Regional Europe charcot-marie-tooth disease...... Working to support those who are affected by charcotmarie-tooth disease, also knownas Hereditary Motor and Sensory Neuropathy or Peroneal Muscular Atrophy.
    http://www.cmt.org.uk/
    CMT United Kingdom Working to support those who are affected by Charcot-Marie-Tooth Disease, also
    known as Hereditary Motor and Sensory Neuropathy or Peroneal Muscular Atrophy. Registered Charity
    No. 327971 Welcome to the website of the support group for people who are affected by Charcot-Marie-Tooth Disease, also known as Hereditary Motor and Sensory Neuropathy or Peroneal Muscular Atrophy. Coping with any medical condition for life is a daunting prospect, but is far more difficult if you can find little information about it or support. This is a problem faced by many people with CMT. Learning to cope with it often means a long search for answers and help. Our website, whilst it will not provide all of the answers, aims to perhaps give you a fresh insight into the condition as well as positive advice about how to live with it. There is also details of the CMT Book which contains a lot more information on CMT. Why not become a member of CMT United Kingdom and enjoy the benefits we are able to offer - ranging from the CMT book 'Charcot-Marie-Tooth Disease - A Practical Guide' through to local support groups, and of course CMT United Kingdom are always there to provide informed personal guidance if you need it.

    11. NINDS Charcot-Marie-Tooth Disorder Information Page
    Information page compiled by National Institute of Neurological Disorders and Stroke.Category Health Conditions and Diseases charcot-marie-tooth disease...... charcotmarie-tooth disease Fact Sheet. charcot-marie-tooth disease fact sheet developedby the National Institute of Neurological Disorders and Stroke (NINDS).
    http://www.ninds.nih.gov/health_and_medical/disorders/charcot_doc.htm
    National Institute of Neurological Disorders and Stroke Accessible version Science for the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system Browse all disorders Browse all health
    organizations
    More about
    Charcot-Marie-Tooth Disorder
    Studies with patients Research literature Press releases
    Search NINDS... (help) Contact us My privacy NINDS is part of the
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    Health
    NINDS Charcot-Marie-Tooth Disorder Information Page
    Reviewed 07-08-2002 Get Web page suited for printing
    Email this to a friend or colleague

    Table of Contents (click to jump to sections) What is Charcot-Marie-Tooth Disorder?
    Is there any treatment?

    What is the prognosis?
    What research is being done? ... Additional resources from MEDLINEplus What is Charcot-Marie-Tooth Disorder? Is there any treatment? There is no cure or specific treatment for CMT. Proper foot care including custom-made shoes and leg braces may minimize discomfort and increase function. Physical therapy and moderate activity are often recommended to maintain muscle strength and endurance. For some patients, surgery may be beneficial. What is the prognosis?

    12. Charcot-Marie-Tooth Disease Fact Sheet
    What is charcotmarie-tooth disease? What are the symptoms of Charcot-Marie-Toothdisease? The neuropathy of CMT affects both motor and sensory nerves.
    http://www.ninds.nih.gov/health_and_medical/pubs/CMT.htm
    National Institute of Neurological Disorders and Stroke Accessible version Science for the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system Browse all disorders Browse all health
    organizations
    More about
    a disorder
    Studies with patients Research literature Press releases
    Search NINDS... (help) Contact us My privacy NINDS is part of the
    National Institutes of

    Health
    Charcot-Marie-Tooth Disease Fact Sheet Get Web page suited for printing
    Email this to a friend or colleague

    Request free mailed brochure
    Table of Contents
    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.

    13. Charcot-Marie-Tooth Disease
    charcotmarie-tooth disease. Synonym Peroneal Muscular Atrophy, Hereditary Motorand Sensory Neuropathy. charcot-marie-tooth disease on-line discussion groups.
    http://www.familyvillage.wisc.edu/lib_cmtd.htm
    Charcot-Marie-Tooth Disease
    Synonym: Peroneal Muscular Atrophy, Hereditary Motor and Sensory Neuropathy
    Who to Contact
    Where to Go to Chat with Others

    Learn More About It

    Web Sites
    ...
    Search AltaVista for "Charcot-Marie-Tooth Disease"
    Who to Contact
    CMT International
    1 Springbank Drive
    St. Catharines, Ontario, Canada L2S 2K1
    Fax: [905] 687-8753
    E-mail: CMTINT@VAXXINE.COM
    CMT International provides support and information to persons who have Charcot-Marie-Tooth disease, their families, caregivers and professionals. They work with medical and research advisors, who constantly update research news and views as well as explore new treatment possibilities. CMT International publishes a bi-monthly newsletter which includes tips for parents of children with Charcot-Marie-Tooth disease, student scholarship applications and sharing information for seniors. There is also a continual update of a list of drugs that can make CMT worse. They also publish pamphlets and booklets on various aspects of CMT.
    Charcot-Marie-Tooth Association (CMTA)
    Crozer Mills Enterprise Center
    601 Upland Avenue Upland, PA 19015 USA

    14. Charcot-Marie-Tooth Disease
    charcotmarie-tooth disease On-Line Discussion Groups. Mailing Lists. ChatRooms. Chat Room at MGH Scroll down to charcot-marie-tooth disease.
    http://www.familyvillage.wisc.edu/lists/charcot.htm
    Charcot-Marie-Tooth Disease
    On-Line Discussion Groups
    Mailing Lists
    MD-LIST
    Created as a forum for exchanging information about muscular dystrophy among patients, family, and friends. People interested in CMT are welcome.
    To subscribe, send a message to:
    MD-List-Request@Basix.COM

    In the body of your message type:
    SUBSCRIBE MD-List
    Web Boards
    Chat Rooms
    If you know of an on-line discussion group that should be added to the list, please send a note to Linda Rowley at: rowley@waisman.wisc.edu Last updated 19-August-1997 by rowley@waisman.wisc.edu.

    15. Hospital Practice: Charcot-Marie-Tooth Disease
    charcotmarie-tooth disease A Gene-Dosage Effect Lupski JR et al DNA duplicationassociated with charcot-marie-tooth disease type 1A. Cell 66219, 1991.
    http://www.hosppract.com/genetics/9705gen.htm
    Molecular Genetics in Clinical Practice
    Charcot-Marie-Tooth Disease:
    A Gene-Dosage Effect
    JAMES R. LUPSKI
    Baylor College of Medicine
    A broad spectrum of inherited neuropathy has been traced to three myelin genes, yet in the two most common disorders, there is no mutated gene. Instead, a gene has an extra or missing copy, as part of a 1.5-megabase DNA duplication or deletion. Eventually, duplications may emerge as a large fraction of all mutations. The discoveries have implications even for acquired disordersincluding carpal tunnel syndrome.
    Dr. Lupski is Cullen Professor of Molecular and Human Genetics, Professor of Pediatrics, and Director, Medical Scientist Training Program, Baylor College of Medicine, Houston. In 1886, the French physicians Jean Martin Charcot and Pierre Marie, and independently the English physician Howard Henry Tooth, described an insidious, slowly progressive atrophy of distal limb muscles that would eventually be recognized as the most common inherited disorder of the peripheral nervous system. It is also among the most common of all genetic disorders, affecting one person in 2,500. Characteristically, the illness becomes evident during the first two decades of life. Often, patients are liable to trip and sprain their ankles, and footdrop forces them to lift the knee, resulting in an equine gait. Eventually, pes cavus appears, and distal muscle atrophy may cause a stork-leg appearance. Weakness of hand muscles usually begins later; in severe cases, claw-like deformity develops.

    16. MEL: Charcot-Marie-Tooth
    charcotmarie-tooth disease. Charcot-Marie-Tooth Association; CMT News (Charcot-Marie-ToothDisease); Family Village on charcot-marie-tooth disease; Tooth Disease;
    http://mel.lib.mi.us/health/health-charcot.html

    Michigan.gov Home
    HAL Home MeL Internet MeL Magazines and eBooks Health Information Resources About the Health Collection Back to the Health Index Medline Evaluating Health Information ... Michigan Health and Hospitals
    Charcot-Marie-Tooth Disease
    See also the MEL Muscular Dystrophy Page
    Back to the Neurological Disorders index page

    Selector and Collection Librarian: Metta Lansdale ( lansdale@mel.org

    17. HealthlinkUSA Charcot-marie-tooth Disease Links
    AhHa. Click here for page 1 of charcot-marie-tooth disease informationfrom the HealthlinkUSA directory. Save on Drugs Here. Accutane;
    http://www.healthlinkusa.com/67ent.htm

    18. Charcot-marie-tooth Disease; Treatment, Prevention, Cure
    charcotmarie-tooth disease Search here for information which may include treatment,diagnosis, prevention, support groups, email lists, messageboards
    http://www.healthlinkusa.com/content/67.html
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    19. Charcot-Marie-Tooth Disease Survey And Information
    Charcot Marie Tooth DiseaseDiagnosis,Rehabilitation,Survey Information. CMT DrugAlerts, CMT Journal Articles,. ****PLEASE READ DISCLAIMER*****.
    http://www.geocities.com/dgosling_rn/
    We subscribe to the HONcode principles of the Health On the Net Foundation and the Medinex Code Of Online Excellence
    Check Your Drugs
    for interactions with other drugs.
    CMT - What is it?

    CMT Internet Links

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    Preliminary Results
    Diagnosis of CMT

    Discount Medical Books
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    MDA Support
    for CMTers Medical Books and Medical Supplies "Numb Toes & Aching Soles": Book Review" "Problem With AFOs In CMT" Research Projects in CMT ... Website Awards "Charcot-Marie-Tooth Disease - Survey and Information" This Site was created and is maintained and funded by Dorothy B. Gosling Reg.N. and Others have donated their time, money and expertise for the benefit of all CMTers. Some Web Page Design features supplied by Webmaster Email: D. B. Gosling This page has been viewed times. Changes last made on: Monday, November 26, 2001 6:08:11 PM

    20. CMT - Charcot Marie Tooth Disease
    CMT Charcot Marie Tooth Disease In Memory of Barbara Coupe/CMT - 12/30/98. TheInternet helps folk with charcot-marie-tooth disease face it head on.
    http://www.naotd.org/cmt.htm

    CMT - Charcot Marie Tooth Disease
    In Memory of Barbara Coupe/CMT - 12/30/98
    Charcot-Marie-Tooth disease (CMT) is named after the three doctors who first described it in 1886, Professor Jean-Martin Charcot (pronounced sharko)(1825-1893), his student, Pierre Marie (1853-1940), who both worked in Paris at the Hospital de Salpetriere named after the former gunpowder factory site where it still stands, and Dr. Howard Tooth (1926-1956) of London. CMT is primarily a disease of the nerves, whereby the myelin or insulating sheath of myelin on the nerves does not stay intact and the messages from the brain to the muscles through the nerves are not carried properly. It differs from muscular dystrophy in that people who have CMT are born with normal muscles. The muscles atrophy because the CMT affected nerves that serve them cannot properly send the message from the brain for them to move. Therefore, muscles can atrophy even though they are being used. It is also called peroneal muscular atrophy (PMA) because the peroneal muscle down the front of the shin that enables you to pull your foot up, is usually the first muscle to be affected. CMT also has a third and more recent name, hereditary motor and sensory neuropathy(HMSN). This name more accurately describes the syndrome because it is hereditary, can affect both or either the ability to move (motor) or the ability to feel (sensory). CMT can be inherited three ways but most cases are inherited autosomal dominate pattern meaning it comes directly down a line from parent to child. In this form of inheritance there is a 50/50 chance at each conception that the child will have CMT. There is also 'spontaneous mutation', where there has never been any sign of the disease in family history, but one, or both parents have carried the gene recessively.

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