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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

AAEM - Patient Resources - Hereditary Motor Sensory Neuropathy
Patient Resources hereditary motor sensory neuropathy. ?. Membership Directory
http://www.aaem.net/aaem/patientInfo/hmsn.cfm

Extractions: List Rental HMSN is an inherited, progressive disease of the nerves with weakness and numbness more pronounced in the legs than the arms. Physical therapy, braces, and orthopedic surgery may help manage these symptoms. Most people with HMSN can walk throughout their life and are self-sufficient. For More Information: Charcot-Marie-Tooth Disease - www.cmtint.org National Organization for Rare Disorders (NORD) - www.rarediseases.org National Society for Genetic Counselors (NSGC) - www.nsgc.org Hereditary Disease Foundation - www.hdfoundation.org Alliance of Genetic Support Groups - www.geneticalliance.org To Main Patient Resources Page 421 First Avenue SW, Suite 300 East
Hereditary Motor-Sensory Neuropathy
hereditary motorSensor neuropathy is also known as Charcot-Marie-Tooth Disease.
http://www.tylermedicalclinic.com/hereditary_motor-sensory_neuropathy.htm

Extractions: The Tyler Medical Clinic Assisted Conception - Affordable Infertility Treatments - List of Diseases - Hereditary Motor-Sensory Neuropathy Hereditary Motor-Sensor Neuropathy is also known as Charcot-Marie-Tooth Disease. For more information, please see the Charcot-Marie-Tooth Disease page. Click here for more information on PGD Click here to learn about other diseases document.write('<');document.write('! '); The contents of The Tyler Medical Clinic Site, such as text, graphics, images, and other material ("Content") are for informational purposes only. The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on The Tyler Medical Clinic Site!
Hereditary Sensory And Motor Neuropathy - General Practice Notebook
medical information from General Practice Notebook. hereditary sensoryand motor neuropathy. CharcotMarie-Tooth disease is an autosomal
http://www.gpnotebook.co.uk/cache/-107347945.htm
Myotonic Dystrophy Associated With Hereditary Motor And Sensory Myotonic Dystrop
hereditary motor and sensory neuropathy. A Medical Encyclopedia Article provided by North Arundel Hospital
http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_109/Issue_06/1091149.sg
Neuropathy, Hereditary Sensory, Type II
on this disorder, choose hereditary sensory neuropathy Type I symptoms may involvesensory, motor, reflex, or on these disorders, choose neuropathy as your
http://bchealthguide.org/kbase/nord/nord798.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 II is a rare genetic disorder that usually begins in childhood. Major symptoms include inflammation of the fingers or toes especially around the nails, usually accompanied by pus and infection (paronychia, whitlows), ulcers (open sores) of the fingers and on the soles of the feet, and a loss of sensation noticeable in both arms and legs.
Hereditary Motor Sensory Neuropathies: Charcot-Marie-Tooth
Antibody Biopsy. Patient Information. hereditary motor sensory NEUROPATHIES (HMSN; CMT) D) KCC3; 15q13. Ataxia with neuropathy TDP1; 14q31. Giant axonal Gigaxonin; 16q24
http://www.neuro.wustl.edu/neuromuscular/time/hmsn.html
Health Library - Neuropathy, Hereditary Sensory, Type I
hereditary sensory neuropathy Type I (HSN I) is a hereditary sensory Neuropathiesof various types may attack a symptoms may involve sensory, motor, reflex, or
http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h
HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH DEAFNESS
Features Listed For hereditary motor AND sensory neuropathy WITH DEAFNESS.McKusick 214370. Deafness, sensorineural; High arches of
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?779
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
Arch Neurol -- Page Not Found
Arch Neurol. 56;1195, October 1999, hereditary motor and SensoryNeuropathy The Plot Thickens, David Pleasure, MD.
http://archneur.ama-assn.org/issues/v56n10/ffull/ned8479.html

Extractions: The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"
Arch Neurol -- Page Not Found
hereditary motor and sensory neuropathy Type 2C Is Genetically Distinct From Types2B and 2D Author Information Masaaki Nagamatsu, MD; Robert B. Jenkins, MD
http://archneur.ama-assn.org/issues/v57n5/abs/noc8450.html

Extractions: The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"
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.
BENCHMARK Analysis Of Hereditary Motor And Sensory Neuropathy,
BENCHMARK analysis of hereditary motor and sensoryneuropathy, Lom type, G2D Home. GO TO
http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U7998
AAEM - Bundles
CR17 Peripheral neuropathy in Monoclonal Gammopathy of Undetermined SignificanceCR20 hereditary motor and sensory neuropathy, Type I CR30 Multifocal motor
http://www.aaem.net/aaem/publications/bundles.cfm

Extractions: Brochures Bundles Case Reports CD-ROMs ... Download Brochures Misc. Information CME Information and Answers Key to Abbreviations AAEM Suggested Reference List The AAEM Education Committee developed the following bundles to serve as an aid in selecting publications of interest. Use the lists to pick out individual titles to purchase within a particular topic or order an entire bundle at a special package rate. ... aaem@aaem.net
Healthlink Template
neuropathy','Proximal hereditary motor neuropathy Type I','Type V hereditary motorand sensory neuropathy','hereditary motor sensory neuropathy with Pyramidal
http://oci.mcw.edu/html-test/HL-2002/health_static/text-search-fulllist.php?neur
Neuropathies, Hereditary Motor And Sensory
CharcotMarie-Tooth disease CMTnet; neuropathy, motor-sensory, TYPE II, WITH DEAFNESSAND MENTAL RETARDATION. Optic Atrophy, hereditary Search PUBMED for Optic
http://www.ohsu.edu/cliniweb/C10/C10.772.587.html
Peripheral Nervous System Diseases
Links to information about peripheral nervous system diseases by Cliniweb International.Category Health Conditions and Diseases Peripheral Nervous System hereditary motor sensory Neuropathies (HMSN) Washington U. neuropathy,motorsensory, TYPE II, WITH DEAFNESS AND MENTAL RETARDATION;
http://www.ohsu.edu/cliniweb/C10/C10.772.html
EMedicine - Hereditary Motor And Sensory Neuropathies : Article Excerpt By: Aami
and Sottas, 1893). More recent nomenclature designated CMT as hereditarymotor and sensory neuropathy (HMSN). Recent advances in
http://www.emedicine.com/neuro/byname/hereditary-motor-and-sensory-neuropathies.

Extractions: (advertisement) Synonyms, Key Words, and Related Terms: Charcot-Marie-Tooth disease type 1B, CMT1B, CMT type 1B, hereditary motor and sensory neuropathy 1B, hereditary motor and sensory neuropathy type 1B, HMSN1B, peroneal muscular atrophy, Dejerine-Sottas syndrome, DSS, hereditary motor and sensory neuropathy type 3 Background: Charcot-Marie-Tooth (CMT) disease was first recognized independently in France and Great Britain (Charcot and Marie, 1886; Tooth, 1886). A few years later, a more severe form of inherited neuropathy was described (Dejerine and Sottas, 1893). More recent nomenclature designated CMT as hereditary motor and sensory neuropathy (HMSN). Recent advances in genetic research have identified several types of HMSN, which correspond with specific genetic mutations. In 1968, Dyck and Lambert created a broader classification system, which is as follows: This article discusses only HMSN types 1, 2, and 3 because these are the most commonly occurring hereditary neuropathies. Other forms of HMSN are extremely rare.
Peripheral Neuropathy
disease CMAP = Compound muscle action potential SNAP = sensory nerveaction potential. hereditary motorsensory neuropathy (HMSN),
http://www.athenadiagnostics.com/site/content/diagnostic_ed/neuro_disorders/peri

Extractions: Peripheral neuropathy (PN) affects two million people in the U.S., typically middle-aged and elderly individuals. It is a neurological disorder that affects the sensory, motor and/or autonomic nerves, and is caused by abnormal function of these nerves due to various etiologies. These disorders can originate from numerous causes, such as diabetes, alcoholism, HIV, toxin exposure, metabolic abnormalities, vitamin deficiency, or adverse effects of certain drugs. However, after evaluations for the etiologies of these PNs are performed, 32-70% of all peripheral neuropathies remain idiopathic. With the development of autoimumme and genetic tests, these idiopathic peripheral neuropathies can often be diagnosed. Autoimmune Peripheral Neuropathy Symptoms of an autoimmune peripheral neuropathy may include weakness, cramping, decreased tendon reflexes, numbness, tingling, and pain affecting the arms and/or legs. Clinically, peripheral neuropathies are classified according to various characteristics: symmetric or asymmetric, proximal or distal, acute or chronic, slowly progressive or rapid onset, affecting one (mononeuropathy) or many nerves (polyneuropathy). Upon electrophysiological examination, assessment of a neuropathy can be further classified, depending on which part of the peripheral nervous system is affected, such as the axon or myelin sheath. Peripheral neuropathy can be demyelinating, axonal, or both, as determined by electromyography (EMG) and nerve conduction studies (NCS).
Neurogenetics - Hereditary Motor-Sensory Neuropathies (HMSN)
Neurogenetics hereditary motor-sensory Neuropathies (HMSN). Request Reprint,Felice, KJ et al., hereditary neuropathy with Liability to Pressure Palsies in
http://www.athenadiagnostics.com/site/content/diagnostic_ed/references/hmsn.asp

Extractions: Reprint Felice, K.J. et al., Hereditary Neuropathy with Liability to Pressure Palsies in Children. Pediatric Neurology 1999; 21:818-821. Chapon, F.P. et al., Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene. Journal of Neurology, Neurosurgery, and Psychiatry 1999; 66:779-782. England, J.D. Entrapment Neuropathies. Current Opinion in Neurology 1999; 12:597-602. Scherer, S.S. and Fischbeck, K.H. Is CMTX an axonopathy? Neurology 1999; 52:432. Parnell, K.J. and Pourmand, R. Evaluation of a Patient Presenting with Foot Drop. Journal of Clinical Neuromuscular Disease 1999; 1(1):41-46. N/A Scherer, S.S. Axonal Pathology in Demyelinating Diseases. Neurology 1999; 1:6-7. Request

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