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

Patient Resources - Hereditary Motor Sensory Neuropathy Membership Directory Practice Issues / Advocacy Employment/Training Career Center Fellowship Listing EDX Courses Training Links ... List Rental Hereditary Motor Sensory Neuropathy (HMSN/Charcot-Marie-Tooth disease) 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 Rochester, MN 55902 Telephone: (507) 288-0100 Fax: (507) 288-1225 E-mail: aaem@aaem.net

22. Hereditary Motor-Sensory Neuropathy hereditary motorSensor neuropathy is also known as Charcot-Marie-Tooth Disease. http://www.tylermedicalclinic.com/hereditary_motor-sensory_neuropathy.htm

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! Last modified: 02/10/03

23. 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

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...

24. 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

Volume 109: January - December 1986 Issue 6: December 1986 Abstract Myotonic dystrophy associated with hereditary motor and sensory neuropathy F Spaans FGI Jennekens JF Mirandolle JB Bijlsma and GC De Gast Pages: Part of the OUP Brain WWW service General Information Click here to register with OUP. This page is maintained by OUP admin Last updated 14 May 97 Part of the OUP Journals World Wide Web service Oxford University Press, 1997

25. 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

document.write(''); var hwPrint=1; var hwDocHWID="nord798"; var hwDocTitle="Neuropathy, Hereditary Sensory, Type II"; var hwRank="1"; var hwSectionHWID="nord798"; var hwSectionTitle=""; var hwSource="cn1.6"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Neuropathy, Hereditary Sensory, Type II 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 Congenital Sensory Neuropathy Hereditary Sensory and Autonomic Neuropathy, Type II (HSAN Type II) Hereditary Sensory Neuropathy Type II Hereditary Sensory Radicular Neuropathy, Type II Radicular Neuropathy, Sensory, Recessive Sensory Neuropathy, Hereditary, Type II Sensory Radicular Neuropathy, Recessive 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 I Peripheral Neuropathy Syringomyelia Roussy-Levy Syndrome General Discussion 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.

26. 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

Front Index Search Links ... Patient Information HEREDITARY MOTOR SENSORY NEUROPATHIES (HMSN; CMT) Dominant CMT 1A : PMP-22; 17p11 CMT 1B : P protein; 1q22 CMT 1C : LITAF; 16p13 CMT 1D HNPP : PMP-22 deletion; 17p11 HMSN 3 (Dejerine-Sottas) PMP-22; P Thermosensitive Connexin-31 Recessive CMT 4A : GDA P1; 8q21.1 CMT 4B CMT 4B2 CMT 4C CMT 4D (Lom) ... CMT 4F : Periaxin; 19q13 HMSN 3 (Dejerine-Sottas) P PMP-22 Periaxin HMSN-Russe ... Congenital hypomyelinating P Farber's lipogranulomatosis Glycosylation deficient, Ia Krabbe : GALC; 14q31 MLD : ARSA; 22q13 PMP-22 point mutations Refsum's disease Childhood : PHYH; 10pter-p11.2 Adolescent-Adult Infant HMSN + CNS : Heterogeneous X-linked Connexin-32 Axonal Dominant CMT 2A CMT 2B CMT 2C CMT 2D ... CMT 2E : Neurofilament light chain; 8p21 CMT 2F CMT 2G (HMSN-Proximal): 3q13.1 CMT 2-P : P HMSN 5 : Pyramidal signs HMSN 6 HMSN + Optic atrophy HMSN + Deafness HSMN + Ulcero-mutilation ... AR-CMT2A : Lamin A/C; 1q21 AR-CMT2B AR-CMT + Hoarseness : GDA P1; 8q21.1 AR-CMT + Pyramidal signs Acrodystrophy Andermann (Corpus callosum D Ataxia with neuropathy Giant axonal : Gigaxonin; 16q24

27. 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

28. 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

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. 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

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery MSJAMA Science News Updates Meetings Peer Review Congress 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"

31. 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

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery MSJAMA Science News Updates Meetings Peer Review Congress 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"

32. 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 March 30, 2003 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.

33. 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

34. 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

Bundles 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

35. 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

36. 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

Neuropathies, Hereditary Motor and Sensory Back to previous level Charcot-Marie Disease Search PUBMED for Charcot-Marie Disease: All Review Therapy Diagnosis ... NEUROPATHY, MOTOR-SENSORY, TYPE II, WITH DEAFNESS AND MENTAL RETARDATION Optic Atrophy, Hereditary Search PUBMED for Optic Atrophy, Hereditary: All Review Therapy Diagnosis Refsum Disease Search PUBMED for Refsum Disease: All Review Therapy Diagnosis Spastic Paraplegia, Hereditary Search PUBMED for Spastic Paraplegia, Hereditary: All Review Therapy Diagnosis Werdnig-Hoffmann Disease Search PUBMED for Werdnig-Hoffmann Disease: All Review Therapy Diagnosis ... SPINAL MUSCULAR ATROPHY I; SMA I

37. 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

Peripheral Nervous System Diseases Back to previous level Acrodynia Search PUBMED for Acrodynia: All Review Therapy Diagnosis Amyloid Neuropathies Search PUBMED for Amyloid Neuropathies: All Review Therapy Diagnosis ... Autonomic Nervous System Diseases [5 more specific term/s, 4 more link/s] Search PUBMED for Autonomic Nervous System Diseases: All Review Therapy Diagnosis ... Cranial Nerve Diseases [8 more specific term/s, 31 more link/s] Search PUBMED for Cranial Nerve Diseases: All Review Therapy Diagnosis ... Demyelinating Diseases [2 more specific term/s, more link/s] Search PUBMED for Demyelinating Diseases: All Review Therapy Diagnosis ... Diabetic Neuropathies [1 more specific term/s, 1 more link/s] Search PUBMED for Diabetic Neuropathies: All Review Therapy Diagnosis ... Nerve Compression Syndromes [4 more specific term/s, 4 more link/s] Search PUBMED for Nerve Compression Syndromes: All Review Therapy Diagnosis ... Neuralgia [4 more specific term/s, 20 more link/s] Search PUBMED for Neuralgia: All Review Therapy Diagnosis ... Neuritis [5 more specific term/s, more link/s] Search PUBMED for Neuritis: All Review Therapy Diagnosis ... Neuropathies, Hereditary Motor and Sensory

38. 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.

(advertisement) Excerpt from Hereditary Motor and Sensory Neuropathies 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 Please click here to view the full topic text: Hereditary Motor and Sensory Neuropathies 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: HMSN types 1A and B (dominantly inherited hypertrophic neuropathies) HMSN type 2 (neuronal type of peroneal muscular atrophy) HMSN type 3 (hypertrophic neuropathy of infancy [Dejerine-Sottas]) HMSN type 4 (hypertrophic neuropathy [Refsum] associated with phytanic acid excess) HMSN type 5 (associated with spatic paraplegia) HMSN type 6 (with optic atrophy) HMSN type 7 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.

39. 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

Peripheral Neuropathy 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).

40. 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

Neurogenetics - Hereditary Motor-Sensory Neuropathies (HMSN) Request 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 Reprint Schenone, A. and Mancardi, G.L. Molecular Basis of Inherited Neuropathies. Current Opinion in Neurology 1999; 12:603-616. Request Reprint Birouk, N. et al., X-Linked Charcot-Marie-Tooth disease with connexin 32 mutations: Clinical and electrophysiologic study. Neurology 1998; 50:1074-1082. Sahenk, Z.L. et al., A novel PMP22 point mutation causing HNPP phenotype. Neurology 1998; 51:702-707.

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