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Hereditary Sensory Motor Neuropathy: more detail

Hereditary Motor and Sensory Neuropathy: Webster's Timeline History, 1980 - 2007 by Icon Group International, 2009-04-16
Genetics of hereditary motor and sensory neuropathy and the Costa Rican contribution.(Charcot-Marie-Tooth (CMT)): An article from: Revista de Biología Tropical by Alejandro Leal, 2004-09-01
Charcot-Marie-Tooth Disease: A Practical Guide. Also Known as Hereditary Motor and Sensory Neuropathy and Peroneal Muscular Atrophy. by (No Author), 2000
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
Lipidoses: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Tish, A.M. Davidson, Altha Edgren, 2006

lists with details

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
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
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

Extractions: 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. HMSN Old polio infection Friederich's ataxia Spina bifida 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.
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 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 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
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
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

Extractions: 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. Information on the following diseases can be found in the Related Disorders section of this report: 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.
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
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

Extractions: (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 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
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

Extractions: 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.
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

Extractions: Dictionaries: General Computing Medical Legal Encyclopedia 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
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

Extractions: 11 May 2004 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.
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
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
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

Extractions: 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.
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

Extractions: 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.
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
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
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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