21. Hereditary Sensory-motor Neuropathy Type 6 Information Diseases Database hereditary sensorymotor neuropathy type 6,HSMN type 6,hereditarysensorimotor neuropathy type 6, Disease Database Information. http://www.diseasesdatabase.com/ddb32095.htm

Diseases Database Index Sponsors Contact ... Previous Page Hereditary sensory-motor neuropathy type 6 Information Search 3 synonyms or equivalents were found. Hereditary sensory-motor neuropathy type 6 aka/or HSMN type 6 aka/or Hereditary sensorimotor neuropathy type 6 may cause or feature (Follow link for list) belong(s) to the category of (Follow link for list) No UMLS definitions Hereditary sensory-motor neuropathy type 6: specific sites Send Hereditary sensory-motor neuropathy type 6 to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-02 22:13:54 Metadata Updated 2004-05-22

22. Hereditary Motor And Sensory Neuropathy hereditary motor and sensory neuropathy. A Medical Encyclopedia Article provided by the University of on over 4000 medical topics including hereditary motor and sensory neuropathy http://www.umm.edu/medical-terms/01934.htm

Hereditary motor and sensory neuropathy A Medical Encyclopedia Article provided by the University of Maryland Medical System A resource with information on over 4000 medical topics including: Hereditary motor and sensory neuropathy Previous Next

23. Clinical Neurosciences - Hereditary Motor And Sensory Neuropathy hereditary motor sensory neuropathy (HMSN). Synonyms. Peroneal muscular atrophy;CharcotMarie-Tooth disease; Roussy-Levy syndrome; Dejerine-Sottas disease. http://medweb.bham.ac.uk/http/depts/clin_neuro/teaching/tutorials/hmsn/hmsn.html

Synonyms Peroneal muscular atrophy; Charcot-Marie-Tooth disease; Roussy-Levy syndrome; Dejerine-Sottas disease HMSN is the commonest cause of the peroneal muscular atrophy syndrome consisting of distal leg muscle wasting and weakness, usually with a pes cavus foot deformity. THE DIFFERENTIAL DIAGNOSIS OF PES CAVUS AND LOWER LEG WASTING INCLUDES: HMSN Old polio infection Friederich's ataxia Spina bifida CLINICAL FEATURES The characteristic clinical features include distal wasting of the lower limb muscles (the so-called 'inverted champagne bottle' appearance). The feet show pes cavus and clawing of the toes, with weakness of the feet extensors. The ankle jerks are absent and the plantar reflexes show no response (occasionally they can be extensor). Palpable nerve thickening is found in about 25% of cases and is specific for the demyelinating forms of HMSN. The patient may have a 'high stepping gait' due to bilateral foot drop. There may be wasting of the small muscles of the hand. In general, the presenting symptoms are due to difficulty walking or a foot deformity. The inheritance is usually autosomal dominant, but recessive forms also occur. The video clip (video not ready yet) shows some of these clinical features in 2 affected brothers.

24. Hereditary Sensory And Motor Neuropathy - General Practice Notebook hereditary sensory and motor neuropathy. CharcotMarie-Tooth disease isan autosomal dominant condition characterised by slowly progressive http://www.gpnotebook.co.uk/cache/-107347945.htm

hereditary sensory and motor neuropathy Charcot-Marie-Tooth disease is an autosomal dominant condition characterised by slowly progressive sensorimotor neuropathy. It is the most commonly inherited peripheral neuropathy in the UK. Lifespan is normal. Disability is usually mild. Click here for more information...

25. Hereditary Motor And Sensory Neuropathy - A Medical Reference Article hereditary motor and sensory neuropathy. A Medical Article provided by University of Maryland Medical on over 10 000 medical topics including hereditary motor and sensory neuropathy http://www.umm.edu/dwp/003279.htm

Hereditary motor and sensory neuropathy A Medical Article provided by University of Maryland Medical Center A resource with information on over 10,000 medical topics including: Hereditary motor and sensory neuropathy Previous Next

26. Hereditary Sensory And Motor Neuropathy - General Practice hereditary sensory and motor neuropathy. Medical search. CharcotMarie-Toothdisease is an autosomal dominant condition characterised http://www.gpnotebook.co.uk/medwebpage.cfm?ID=-107347945

27. Neuropathy, Hereditary Sensory, Type I hereditary sensory Neuropathies of various types may attack a single nerve (mononeuropathy Thesesymptoms may involve sensory, motor, reflex, or blood vessel http://my.webmd.com/hw/health_guide_atoz/nord799.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Neuropathy, Hereditary Sensory, Type I Important It is possible that the main title of the report Neuropathy, Hereditary Sensory, Type I is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Acrodystrophic Neuropathy Hereditary Sensory and Autonomic Neuropathy, Type I (HSAN Type I) Hereditary Sensory Neuropathy Type I (HSN I) Hereditary Sensory Radicular Neuropathy, Type I Mutilating Acropathy Radicular Neuropathy, Sensory Sensory Neuropathy, Hereditary, Type I

28. Neuropathy, Hereditary Sensory, Type I Pp. 1019. BIOLOGY AND GENETICS OF hereditary motor AND sensory NEUROPATHIES.U. Suter, et al., Annu Rev Neurosci. 1995, 1845. SYMPATHETIC http://www.bchealthguide.org/kbase/nord/nord799.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord799"; var hwDocTitle="Neuropathy, Hereditary Sensory, Type I"; var hwRank="1"; var hwSectionHWID="nord799"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Neuropathy, Hereditary Sensory, Type I Important It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Acrodystrophic Neuropathy Hereditary Sensory and Autonomic Neuropathy, Type I (HSAN Type I) Hereditary Sensory Neuropathy Type I (HSN I) Hereditary Sensory Radicular Neuropathy, Type I Mutilating Acropathy Radicular Neuropathy, Sensory Sensory Neuropathy, Hereditary, Type I Sensory Radicular Neuropathy Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Charcot-Marie-Tooth Disease Hereditary Sensory Neuropathy Type II Peripheral Neuropathy Syringomyelia Roussy-Levy Syndrome General Discussion Hereditary Sensory Neuropathy Type I (HSN I) is a rare genetic disorder characterized by the loss of sensation, especially in the feet and legs and, less severely, in the hands and forearms. The loss of sensation is caused by abnormal functioning of the autonomic nervous system, which controls responses to pain and temperature as well as other involuntary or automatic body processes.

29. Dorlands Medical Dictionary is familial dysautonomia. sensory and motor neuropathy, hereditary,hereditary motor and sensory n. sensory radicular neuropathy http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

30. EMedicine - Multifocal Motor Neuropathy With Conduction Blocks : Article By Sasa acquired demyelinating sensory and motor polyneuropathy MADSAM) Mononeuritis multiplexhereditary motor sensory neuropathy type 2 hereditary neuropathy with http://www.emedicine.com/neuro/topic724.htm

(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Neurology Neuromuscular Diseases Multifocal Motor Neuropathy With Conduction Blocks Last Updated: January 1, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: MMN, acquired immune-mediated demyelinating neuropathy, amyotrophic lateral sclerosis, ALS, demyelinating injury, axonal injury, anti-GM1 antibodies AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Sasa Zivkovic, MD, MSc , Codirector, Botox Clinic, Assistant Professor, Department of Neurology, Division of Neuromuscular Diseases, University of Pittsburgh Medical School Sasa Zivkovic, MD, MSc, is a member of the following medical societies: American Academy of Neurology Editor(s): Paul E Barkhaus, MD , Director, Division of Neuromuscular Diseases, Milwaukee Veterans Administration Medical Center; Professor, Department of Neurology, Medical College of Wisconsin; Francisco Talavera, PharmD, PhD

31. NINDS Hereditary Neuropathies Information Page disorders, including hereditary motor and sensory neuropathy, hereditary sensoryneuropathy, hereditary motor neuropathy, and hereditary sensory and autonomic http://www.ninds.nih.gov/health_and_medical/disorders/neuropathy_hereditary.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 Hereditary Neuropathies Studies with patients Research literature Press releases Search NINDS... (help) Contact us My privacy NINDS is part of the National Institutes of Health NINDS Hereditary Neuropathies Information Page Synonym(s): Neuropathy - Hereditary Reviewed 05-06-2003 Get Web page suited for printing Email this to a friend or colleague Table of Contents (click to jump to sections) What are Hereditary Neuropathies? Is there any treatment? What is the prognosis? What research is being done? ... Related NINDS Publications and Information What are Hereditary Neuropathies? Hereditary neuropathies are a group of inherited disorders of the peripheral nervous system. Within the group there are 4 subcategories of disorders, including hereditary motor and sensory neuropathy, hereditary sensory neuropathy, hereditary motor neuropathy, and hereditary sensory and autonomic neuropathy.

32. Hereditary Motor And Sensory Neuropathy Definition Of Hereditary Motor And Senso Definition of hereditary motor and sensory neuropathy in the Dictionaryand Thesaurus. hereditary hereditary motor and sensory neuropathy. Word http://www.thefreedictionary.com/hereditary motor and sensory neuropathy

Dictionaries: General Computing Medical Legal Encyclopedia hereditary motor and sensory neuropathy Word: Word Starts with Ends with Definition Noun hereditary motor and sensory neuropathy - 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 Charcot-Marie-Tooth disease neuropathy - any pathology of the peripheral nerves Legend: Synonyms Related Words Antonyms Some words with "hereditary motor and sensory neuropathy" in the definition: ataxia ataxy Charcot-Marie-Tooth disease cortical area ... Recurrent sensibility Previous General Dictionary Browser Next Hereditability Hereditable Hereditably ... Heremitical Full Dictionary Browser herediatry spinal ataxia Hereditability Hereditable Hereditably ... Hereditaments (law) hereditarianism Hereditarily Hereditarily finite set (enc.) Hereditary Hereditary (law) Hereditary (enc.)

33. Charcot-Marie-Tooth Hereditary Neuropathy Overview Clinical manifestations of CharcotMarie-Tooth hereditary neuropathy also calledhereditary motor/sensory neuropathy (HMSN) result from involvement of http://www.geneclinics.org/profiles/cmt/details.html

Charcot-Marie-Tooth Hereditary Neuropathy Overview [CMT] Author: Thomas D Bird, MD About the Author Initial Posting: 28 September 1998 Last Revision 11 May 2004 Summary Disease characteristics. Charcot-Marie-Tooth (CMT) hereditary neuropathy refers to a group of disorders characterized by a chronic motor and sensory polyneuropathy. The typical patient has distal muscle weakness and atrophy often associated with mild to moderate sensory loss, depressed tendon reflexes, and high-arched feet. The CMT hereditary neuropathies are categorized by mode of inheritance and causative gene or chromosomal locus Diagnosis/testing. The genetic neuropathies need to be distinguished from the many causes of acquired (non-genetic) neuropathies. Clinical diagnosis is based on family history and characteristic findings on physical examination, EMG/NCV testing, and occasionally on sural nerve biopsy. Molecular genetic testing is available in clinical laboratories for diagnosis of CMT1A (MPZ) (NEFL) , CMTX , and CMT4F (PRX) Genetic counseling CMT hereditary neuropathy syndrome can be inherited in an autosomal dominant autosomal recessive , or X-linked manner.

34. Peripheral Neuropathy -- Printable Tables MarieTooth disease types 1,2,3 and X B. Familial amyloidosis C. hereditary predispositionto IV. Asymmetric Generalized sensory and motor Polyneuropathies. http://www.clevelandclinicmeded.com/diseasemanagement/neurology/pneuro/pneurotab

TITLE: PERIPHERAL NEUROPATHY AUTHORS: ROBERT W. SHIELDS MD Department of Neurology PUBLISHED: FEBRUARY 9, 2004 Table 1: Peripheral Neuropathy Syndromes I. Acute-Subacute Generalized Polyneuropathies A. Sensorimotor 1. Acute motor and sensory axonal neuropathy syndrome 2. Alcohol/nutritional 3. Toxins (metals) 1. Guillain-Barre syndrome 2. Acute motor axonal neuropathy syndrome 3. Porphyria 4. Diphtheria 5. Toxins (dapsone, vincristine) C. Sensory 1. Paraneoplastic/autoimmune (anti-Hu associated) 2. Vitamin B toxicity 3. Toxins (cisplatin) 4. Human immunodeficiency virus II. Chronic Generalized Symmetric Polyneuropathies A. Sensorimotor 1. Diabetes 2. Uremia 3. Alcohol/nutritional 4. Dysproteinemias 5. Connective tissue diseases

35. Journal Articles Written About Charcot-Marie-Tooth Disease Your Local Medical Library, Some Abstracts of the Articles May Be Found By SearchingMedline for Charcot Marie Tooth or hereditary motor sensory neuropathy . http://www.geocities.com/dgosling_rn/journal2.html

******PLEASE READ and We subscribe to the HONcode principles of the Health On the Net Foundation and the Medinex Code Of Online Excellence Please note that ALL of the articles listed on these pages are old. The reason I have left them here as a reference is that some of the old research done a number of years ago, has not been repeated or updated. Some people may find these articles have some value in their search for information about Charcot Marie Tooth Disease. The Full Text of the Following Articles Can Be Found At Your Local Medical Library, Some Abstracts of the Articles May Be Found By Searching Medline for "Charcot Marie Tooth" or "Hereditary Motor Sensory Neuropathy" Text Only and Version To Print Pages: General Overviews of CMT Anaesthesia And The CMT Patient Autosomal Recessive CMT Bone Density and CMT ... Vocal Cords In CMT Cold Stress in CMT "Abnormal responses to cold stress in Charcot-Marie-Tooth I syndrome"; Williams LL, et al.; Arch Phys Med Rehabil. 1994 Jul;75(7):787-91. Diagnostic Tests in CMT "Ultrasound of radial, ulnar, median, and sciatic nerves in healthy subjects and patients with hereditary motor and sensory neuropathies", Heinemeyer O.et al; Ultrasound Med. Biol. 1999 25/3 (481-485)

36. Research Reports- Hereditary Motor Sensory Neuropathy Impairment Disability Profiles of Neuromuscular Diseases HereditaryMotor sensory neuropathy. By WM Fowler, Jr., MD, GT Carter http://www.rehabinfo.net/rrtc/publications/research_summaries/Hereditary_mo.asp

NIDRR Rehabilitation Research and Training Center in Neuromuscular Diseases (RRTC/NMD) Search Site Path: Home rrtc publications Hereditary_mo.asp June 2, 2004 Hereditary Motor Sensory Neuropathy. By W.M. Fowler, Jr., MD, G.T. Carter, MD, D.D. Kilmer, MD, E.R. Johnson, MD, S. Aitkens, N. Wright, and T. Abresch, MS. The purpose of this study was to develop a comprehensive impairment and disability profile for HMSN. Impairment was evaluated by measurements of strength, contractures, spine deformity, cardiac function, pulmonary function and intellectual capacity. Impairment frequently leads to disability. Disability evaluations consisted of measures of mobility and upper extremity function, cardiopulmonary adaptations, cardiac and pulmonary disease, and psychosocial adjustment. One hundred and twenty patients followed in a regional Neuromuscular Disease (NMD) Clinic, 1982-1992, were reviewed. Sixty-eight were males and fifty-two were females. Age was 44 ± 18 years and disease duration 33 ± 14 years at the time of the first clinic visit. Six percent were non-ambulatory, and age at loss of ambulation was 29 ± 14 years. Only two were known to have died during the ten year period. All participants from the clinic did not receive all measurements so the individuals in each of the impairment or disability profiles would be considered as samples of the larger clinic population.

37. Disorder Information - Hereditary Motor And Sensory Neuropathy With Agenesis Of hereditary motor and sensory neuropathy with Agenesis of the CorpusCallosum. This brochure on hereditary motor and sensory neuropathy http://www.mdac.ca/english/disorder-info/disorder-info-26_neuropathy.htm

Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum This brochure on Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum presents an overall description of the symptoms associated with the disorder and of its effects on the people affected at different stages of their lives. Should you have any questions after this reading, please contact the resource services listed at the end of this document. What is Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum? What are the symptoms of HMSN/ACC? How does the disease progress? What causes HMSN/ACC? How can I know whether I am a carrier of the HMSN/ACC gene? ... What are the main resources available to people living with HMSN/ACC and their families in the populations showing high incidence of the disease? What is Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum? Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum (HMSN/ACC) is a progressive hereditary neuromuscular disorder that mainly affects people from the Saguenay-Lac-St-Jean (SLSJ) and Charlevoix regions of Quebec, as well as people whose ancestors are native of these regions. Some cases of HMSN/ACC have also been identified in others countries. HMSN/ACC is responsible of the degeneration of the peripheral nerves involved in both body movement and the perception of sensations. Irregularities are also observed in the brain of the people living with the HMSN/ACC, predominantly in the anatomical structure interconnecting the two cerebral hemispheres, known as the corpus callosum. The corpus callosum is found to be totally absent in 57.8% of patients, partially absent in 9.4% of them, and normally present in 32.8% of people living with the disorder.

38. NORD - National Organization For Rare Disorders, Inc. These symptoms may involve sensory, motor, reflex, or blood vessel (vasomotor)functions. Organizations related to neuropathy, hereditary sensory, Type I http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Neuropathy, H

39. V, HMSN (Hereditary Motor And Sensory Neuropathy Type V) : On Medical Dictionary V, HMSN (hereditary motor and sensory neuropathy Type V) defined on theFree Online Medical Dictionary. Medical terminology definitions http://www.online-medical-dictionary.org/?q=V, HMSN (Hereditary Motor and Sensor

40. HMSN V (Hereditary Motor And Sensory Neuropathy Type V) : On Medical Dictionary HMSN V (hereditary motor and sensory neuropathy Type V) defined on the Free OnlineMedical Dictionary. HMSN V (hereditary motor and sensory neuropathy Type V). http://www.online-medical-dictionary.org/?q=HMSN V (Hereditary Motor and Sensory

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