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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

61. Charcot-Marie-Tooth Disease By Anonymous
I have CMT (charcotmarie-tooth disease), a genetic neurological disease that causes deformities in the extremities and pain in the hands and feet.
http://www.rxmarihuana.com/shared_comments/Charcot_Marie_Tooth.htm
Charcot-Marie-Tooth Disease by Anonymous

62. Closing In On Treatment For Charcot-Marie-Tooth Disease?
Interuniversity Institute of Biotechnology Closing in on treatment for charcotmarie-tooth disease? Charcot-Marie-Tooth (CMT) is
http://www.eurekalert.org/pub_releases/2004-05/vfii-cio050704.php
Public release date: 7-May-2004
Contact: Ann Van Gysel
ann.vangysel@vib.be

VIB, Flanders Interuniversity Institute of Biotechnology
Closing in on treatment for Charcot-Marie-Tooth disease?
Charcot-Marie-Tooth (CMT) is a hereditary disorder of the peripheral nervous system that strikes 1 person in every 2500. Increasing debilitation of the muscles ultimately leads to their disappearance in the lower legs, feet and hands. Now, researchers from VIB (the Flanders Interuniversity Institute for Biotechnology) have discovered a piece of the molecular puzzle of this disease. Two small 'heat shock' proteins turn out to be crucial - faults in the coding genes lead to the disease. Additional research has shown that these proteins play an important role in many other neurodegenerative disorders as well. This research moves us a step closer to the development of new therapies. CMT, a serious disorder without a cure CMT, the most common hereditary disorder of the peripheral nervous system, leads to debilitation of the muscles in the lower legs, feet and hands. The clinical picture is extremely variable, but older patients sometimes require a wheelchair. Today, only supportive treatment is available; there are still no effective therapies to retard or stop the progress of the disease. More insight into the molecular processes of this disease is essential for diagnosis and potential treatment. And exploration of the genes involved is a crucial step in this. VIB research findings Joy Irobi and her colleagues - under the direction of Vincent Timmerman and Peter De Jonghe of the Department of Molecular Genetics, University of Antwerp - are concentrating on the genetic and biological study of hereditary disorders of the peripheral nervous system. The largest cells in our body, our peripheral neurons can be 1 meter long in bundles of nerve fibers extending from the spinal cord to the feet.

63. Charcot-marie-tooth Disease
Ailment Name charcotmarie-tooth disease. Join this Community get help by emailing and chatting to others, and sharing information and experiences,
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64. Charcot-Marie-Tooth Disease Survey And Information
charcotmarie-tooth disease - Survey and Information © 1997-2003 All rights reserved. This Site was created and is maintained
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CMT - What is it?

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This Site was created and is maintained and funded by Dorothy B. Gosling Reg.N. and Privacy Policy 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 Changes last made on: Monday, May 24, 2004

65. Charcot-Marie-Tooth Disease
CMTnet charcotmarie-tooth disease Information CMTnet is a repository of information for research and treatment of Charcot-Marie-Tooth (CMT).
http://www.doctorpage.com/findit/Diseases_and_Conditions/Charcot_Marie_Tooth_Dis

doctorpage
Diseases and Conditions Charcot Marie Tooth Disease Displaying listings 1-4
  • CMTUS email support + discussion group for people with CMT A global, private, CMT email discussion group for sharing positive living ideas, practical solutions and new research modalities. 56 Links, polls, open 7 days, 24 hours per day. All with CMT are wellcome! http://www.egroups.com/group/CMTUS CMTnet: Charcot-Marie-Tooth Disease Information 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 extremities. http://www.ultranet.com/~smith/CMTnet.html Charcot-Marie-Tooth Disease National Institutes of Health, Bethesda, Maryland 20892 Written August 1996 Index: : Charcot-Marie-Tooth disorder is an inherited neurological disease characterized by a slowly progressive ... http://www.ninds.nih.gov/healinfo/DISORDER/charcot/charcot.htm Charcot-Marie-Tooth disease (hereditary) Disease progressive neuropathic muscular atrophy; hereditary peroneal nerve dysfunction; neuropathy - peroneal A slowly progressive, inherited disorder characterized by of tissue in the feet and ... http://www.healthanswers.com/database/ami/converted/000727.html

66. Closing In On Treatment For Charcot-Marie-Tooth Disease?
Closing in on treatment for charcotmarie-tooth disease? 08 May 2004
http://www.medicalnewstoday.com/index.php?newsid=8068

67. NetDoctor.co.uk - Smoking - Ask The Expert
charcotmarie-tooth disease and smoking 28-11-2002. Question. Does having charcot-marie-tooth disease give me more than most a reason to give up smoking?
http://community.netdoktor.com/ccs/uk/smoking/coping/expert/article.jsp?articleI

68. Epilepsy, Charcot Marie Tooth Disease By NYERRN
Epilepsy and Charcot Marie Tooth Disease. Charcot Marie Tooth Disease. CharcotMarie-Tooth Association. Family Village on charcot-marie-tooth disease.
http://www.nyerrn.com/neuro/3.htm
Epilepsy and Charcot Marie Tooth Disease
Charcot Marie Tooth Disease
Charcot-Marie-Tooth Association CMTnet - CMTnet provides information for both the medical and non-medical communities on Charcot-Marie-Tooth (CMT). CMT International - (Charcot-Marie-Tooth Disease) Formally known as Charcot-Marie-Tooth Disease/Peroneal Muscular Atrophy International Association, Inc. This site includes information about hereditary neuropathy with liability to pressure palsies (HNPP). Family Village on Charcot-Marie-Tooth Disease Muscular Dystrophy Association - Facts About Charcot-Marie-Tooth Disease (CMT) National Alliance OF The Disabled (NAOTD) CMT - Charcot Marie Tooth Disease National Center for Biotechnology Information National Institute of Neurological Disorders and Stroke - Charcot-Marie-Tooth Disorder National Organization for Rare Disorders (NORD) - Charcot Marie Tooth Disease Summary Neurology Channel -Charcot-Marie-Tooth Disease Return to the Index of Neurology Topics
Epilepsy
American Epilepsy Society - A professional organization of clinicians and researchers. Epilepsy Canada Epilepsy Contact Database Epilepsy Education Association Epilepsy Foundation of America - Includes FAQs and a "News Desk"

69. Genetics Research: Charcot Marie Tooth
charcotmarie-tooth disease Type 1A. Principal Investigator Pragna I. Patel, Ph.D. Autosomal dominant inheritance pattern; Frequency
http://www.bcm.tmc.edu/neurol/research/genes/genes3.html
Charcot-Marie-Tooth Disease Type 1A
Principal Investigator:
Pragna I. Patel, Ph.D.
  • Autosomal dominant inheritance pattern
  • Frequency: ~ 1 in 2,500 (most common inherited peripheral neuropathy)
  • Signs/symptoms include: distal muscle atrophy, decreased nerve conduction velocity, absent deep tendon reflexes, pes cavus, pes planus
  • Our recent discoveries include:
    • CMT1A associated in >70% of patients with a 1.5 million base pair DNA duplication on chromosome 17
    • Peripheral myelin protein 22 (PMP22) gene mapped within the duplication
    • Point mutations in PMP22 also associated with CMT1A

  • Current efforts include studying the regulation of the PMP22 gene and using triplex oligonucleotides as a possible approach for modulating PMP22 expression.
Selected References:
  • Patel, P.I., and Lupski, J.R. Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inherited disease. Trends. Genet., 10:128-133, 1994.
  • Patel, P.I., Roa, B., Welcher, A., Schoener-Scott, R., Trask, B.J., Pentao, L., Snipes, G.J., Garcia, C.A., Francke, U., Shooter, E., Lupski, J.R., and Suter, U. The gene for the peripheral myelin protein PMP-22 gene is a candidate for Charcot-Marie-Tooth disease type 1A. Nature Genetics, 1:159-165, 1992.
  • Lupski, J.R., Montes de Oca-Luna, R., Slaugenhaupt, S., Pentao, L., Guzzetta, V., Trask, B.J., Saucedo-Cardenas, O., Barker, D.F., Killian, J.M., Garcia, C.A., Chakravarti, A., and Patel, P.I. DNA duplication associated with Charcot- Marie-Tooth disease type 1A. Cell, 66:219-232, 1991.
  • 70. Short Description Of Cell Lines. Pathology: Charcot-Marie-Tooth Disease #118200
    Version 4.200205, Short description of cell lines. Pathology charcotmarie-tooth disease 118200 OMIM record. - By selecting the
    http://www.biotech.ist.unige.it/cldb/pat56.html
    Version
    Short description of cell lines.
    Pathology: Charcot-Marie-Tooth disease
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    By selecting the cell line name , you will receive the detailed description of the cell line
    By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
    You can search any term of the list by using the 'Find' utility of your browser
    human, Caucasian
    skin, fibroblast GEIMM
    human, Caucasian
    ...
    By Beatrice...

    71. CHARCOT-MARIE-TOOTH DISEASE
    charcotmarie-tooth disease. Cie Cie Glencross. charcot-marie-tooth disease presents in a variety of clinical forms and presents at different ages.
    http://podiatry.curtin.edu.au/encyclopedia/ciecle/
    CHARCOT-MARIE-TOOTH DISEASE
    Cie Cie Glencross
    Figure 1: Charcot-Marie-Tooth typical cavus foot type and inverted champagne bottle leg
    Back to Encyclopedia Index
    INTRODUCTION
    Scope of the Report
    Aims of the Report
    The report will cover the following areas:
    • Mode of Inheritance
    • Types of Charcot-Marie-Tooth disease
    • Pathogenesis of Charcot-Marie-Tooth disease
    • Pathology of Charcot-Marie-Tooth disease
    • Clinical Features
    • Diagnosis of Charcot-Marie-Tooth disease
    • Conservative and Surgical Treatment of Charcot-Marie-Tooth disease.

    Back to Contents
    OVERVIEW:
    Prevalence
    Mode of Inheritance
    Types
    Back to Contents
    SPECIFICS:
    PATHOLOGENESIS
    Neural Pathogenesis
    Muscular Pathogenesis
    1. The muscles supplied by the longest axon of the Sciatic nerve are affected first.
    2. The muscles showing the least bulk are foremost in showing wasting.
    3. Muscles above the knee are not affected.
    Downey et al (1992) and Mann and Missirian (1983; 1986) support this theory in explaining the pattern of muscle wasting and dysfunction. The intrinsic muscles of the foot are the first to atrophy as a result of their size and innervation by the medial and lateral plantar nerves. The anterior muscles of the leg are next to atrophy presumably as a result of their innervation be the smaller branch of the Sciatic nerve. As a result of the lack of muscle bulk, Peroneus Brevis and Peroneus Tertius atrophy before their counterpart Peroneus Longus. As Charcot-Marie-Tooth disease is progressive, the posterior leg muscle group and the triceps surae may be involved. However, because of the greatest muscle bulk, they are typically the last to atrophy (Downey, 1992).

    72. Muscular Dystrophy Campaign Hereditary Motor And Sensory Neuropathies (HMSN)
    Hereditary Motor and Sensory Neuropathies (HMSN). (Sometimes known as charcotmarie-tooth disease or Peroneal muscular atrophy). December 2000.
    http://www.muscular-dystrophy.org/information/keyfacts/hmsn.html
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    David N Russell
    Hereditary Motor and Sensory Neuropathies (HMSN)
    (Sometimes known as Charcot-Marie-Tooth Disease or Peroneal muscular atrophy) December 2000 From an original written by the late Prof Anita Harding MD, FRCP and revised by Dr D.Hilton-Jones MD, FRCP, for the Muscular Dystrophy Campaign. What are hereditary motor and sensory neuropathies? The term hereditary and sensory neuropathy (HMSN) is used to describe a group of conditions that give rise to weakness and wasting of the muscles below the knees and often those of the hands. Many affected people also have a loss of feeling in the hands and feet, and this is the ‘sensory’ component. The term neuropathy refers to the fact that it is the peripheral nerves (which connect the spinal cord to the muscles, joints and skin, carrying messages in both directions), which do not function normally. As the name implies, these are inherited disorders. Many different names have been used to describe HMSN in the past, and this is rather confusing. They are often referred to as peroneal muscular atrophy, because the peroneal muscle on the outside of the calves are particularly affected. Another commonly used name is Charcot-Marie-Tooth disease, after the three neurologists who first described the condition in 1886. Other names include Dejerine-Sottas disease and hereditary hypertrophic neuropathy. HMSN is now the preferred term, largely because Charcot-Marie-Tooth disease and peroneal muscular atrophy are more general terms used to describe a wider group of conditions including one form of spinal muscular atrophy.

    73. MEDLINE Abstracts Charcot-Marie-Tooth Disease
    Preliminary Study of Large and Small Peripheral Nerve Fibers in charcotmarie-tooth disease, Type I. Hanson P, Deltombe T Am J Phys Med Rehabil 1998; 77(1)45-8
    http://www.medscape.com/viewarticle/431507

    74. Database Search Results
    does not imply endorsement by the US Department of Health and Human Services.. Searched keywords for charcotmarie-tooth disease.
    http://www.health.gov/NHIC/NHICScripts/Hitlist.cfm?Keyword=Charcot-Marie-Tooth D

    75. Health Information Resource Database: CMT International (Charcot-Marie-Tooth Dis
    CMT International (charcotmarie-tooth disease/Peroneal Muscular Atrophy International Association, Inc.). Contact Information. 1 Springback Drive St.
    http://www.health.gov/nhic/NHICScripts/Entry.cfm?HRCode=HR2300

    76. Charcot-Marie-Tooth Disease
    charcotmarie-tooth disease. charcot-marie-tooth disease is an inherited disorder of nerves (neuropathy) that is characterized by
    http://www.sciencedaily.com/encyclopedia/charcot_marie_tooth_disease
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    Charcot-Marie-Tooth disease
    Charcot-Marie-Tooth disease is an inherited disorder of nerves (neuropathy) 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. The disorder is caused by the absence of molecules that are essential for normal function of the nerves due to deficiencies in the structure of the genes coding these molecules. The absence of these chemical substances gives rise to dysfunction either in the axon or the myelin sheath of the nerve cell. Symptoms usually begin in late-childhood or early adulthood. Usually, the initial symptom is foot drop due to involvement of the peroneal nerve, which is responsible from raising the feet, early in the course of the disease. Wasting of muscle tissue of the lower parts of the legs may give rise to "stork leg" appearance. The diagnosis is established by electromyography examination (which shows that the velocity of nerve impulse conduction is decreased and the time required to charge the nerve is increased) and nerve biopsy. There is no treatment to replace the missing chemicals. The disease is named for those who classically described it: Jean-Martin Charcot (1825-1893) and his pupil Pierre Marie (1853-1940) (

    77. BioMed Central PDF Charcot-Marie-Tooth Disease
    To obtain access to IDrugs through your institution use the options below. If you would like information about a personal subscription
    http://www.biomedcentral.com/content/pdf/cd-522764.pdf

    78. Neurological Disorders, Peripheral Nervous System, Charcot-Marie-Tooth Disease
    More charcotmarie-tooth disease Categories » Submit Your Site to the charcot-marie-tooth disease category. Sponsored charcot-marie-tooth disease Sites.
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    79. Charcot-Marie-Tooth Disease (C) Channel
    AZ, charcotmarie-tooth disease, CMT UK is the national support group for people affected by charcot-marie-tooth disease (CMT) and their families and carers.
    http://www.aditus.nhs.uk/Aditus/Patients and Public/A-Z/C/Charcot-Marie-Tooth Di
    Home Patients and Public Staff and Students Resources ... Help Not logged in... Login: Register: Forgotten password Search: home patients and public staff and students resources ... help A-Z Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease is also referred to as Hereditary Motor and Sensory Neuropathy (HMSN) and Peroneal Muscular Atrophy. For more general information on neurological conditions, please visit the neurological disorders homepage Useful Links CMT UK CMT UK is the national support group for people affected by Charcot-Marie-Tooth Disease (CMT) and their families and carers. The website includes:
    • What is CMT
    • Living with CMT
    • A child's guide.
    Documents and Reports There are no Documents or Reports currently defined for this topic. Journals and Databases There are no Journals or Databases currently defined for this topic. Support Groups There are no support groups currently defined for this topic. Events There are no events currently defined for this topic. Select a Subject A B C D ... Z
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    80. Foot Problems In Charcot-Marie-Tooth Disease - CMTworld.org Article
    charcotmarie-tooth disease web site - Kids! Children! Click here! CMT Symptoms Foot Problems in charcot-marie-tooth disease By Dr. Jay Kumar Issue date Mar.
    http://www.cmtworld.org/epublisher/publish/article_0090.php

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    June 2, 2004, 5:35 am You can help! Donate Online now! CMT Symptoms
    Foot Problems in Charcot-Marie-Tooth Disease
    By Dr. Jay Kumar Issue date: Mar. 19/04 Email this article Printer friendly page One of the common problems seen in children and adolescents who have CMT in the 10 to 16-year-old age group, and in young adults, is a cavo-varus foot where there is a high arch and patients walk on the outer border of the foot. All of the pressure goes through the heel and the outer side of the foot, resulting in calluses on the outer border and heel. With time, the big toe on the inner side drops down creating a lot of pressure on the ball of the foot. As the people we see become older, the toes tend to claw resulting in calluses on the knuckles of the toes. Patients present with the following problems:

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