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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

CMT Charcot-Marie-Tooth HMSN Hereditary Motor Sensory Neuropathy
Information, help and support for those with CMT HMSN.
http://www.cmt-support.com/
PharmGKB: Spastic Paraplegia, Hereditary
V); hereditary Autosomal Dominant Spastic Paraplegia; hereditary Autosomal RecessiveSpastic Paraplegia; hereditary motor sensory neuropathy with Pyramidal
http://www.pharmgkb.org/do/serve?objId=PA446141&objCls=Disease
HMSN Best Practice Guidelines (eu)
hereditary motor and sensory neuropathy type I (HMSN I, CMT1) is characterized byseverely slowed motor and sensory nerve conduction velocities (NCV) and signs
http://www.emqn.org/guidelines.php?page=hmsn
Blackwell Synergy - Cookie Absent
hereditary motor and sensory neuropathy with absence of large myelinated fibersdue to absence of large neurons in dorsal root ganglia and anterior horns
http://www.blackwell-synergy.com/links/doi/10.1046/j.1529-8027.2000.00020.x/full

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HIV Report May 2001 - Sensory Neuropathy In HIV/AIDS
lower CD4 count, and concurrent causes of neuropathy including diabetes mellitus,prior cancer chemotherapy, and hereditary sensory motor polyneuropathies.
http://www.hopkins-aids.edu/publications/report/may01_2.html

Extractions: Pathophysiology Risk Related to Specific ART Agents Treatment of HIV-Associated and Dideoxynucleoside-Associated Toxic Sensory Neuropathy "There is no more lively sensation than that of pain; its impressions are certain and dependable..." Marquis de Sade, 1791 Sensory neuropathy occurring in the context of HIV/AIDS has become a frequent complication, particularly in patients treated with dideoxynucleoside antiretrovirals. Sensory neuropathy not only affects the quality of life, but is frequently under-treated, even by expert HIV providers. Increasingly, the occurrence of HIV associated sensory neuropathy limits the choice of HAART regimens by excluding the use of dideoxynucleosides. In addition, the development of neuropathic symptoms, or even the fear of sensory neuropathy, may reduce adherence with antiretrovirals. Finally, peripheral neuropathy may actually be an early marker of mitochondrial dysfunction, which is now believed to contribute to the development of lipodystrophy, lactic acidosis, and other toxicities. Clinical Characteristics Neurology . 1998;52:607]. Other risk factors include age, the presence of wasting syndrome, lower CD4 count, and concurrent causes of neuropathy including diabetes mellitus, prior cancer chemotherapy, and hereditary sensory motor polyneuropathies.
Hereditary Motor And Sensory Neuropathy Mimicking Hansen's Disease.
hereditary motor and sensory neuropathy mimicking Hansen s disease. Indian Journalof Dermatology Venereology and Leprology. 1996 MayJune; 62(3) 189-90.
http://medind.nic.in/imvw/imvw13104.html

Extractions: Extracted from IndMED Somani VK; Sucharita V; Sharma VK; Sita VNVL; Razvi F; Fatima Razvi Department of Skin and VD, Deccan College of Medical Sciences, Princess Esra Hospital, Shah Ali Bunda, Hyderabad. Hereditary motor and sensory neuropathy mimicking Hansen's disease. Indian Journal of Dermatology Venereology and Leprology. 1996 May-June; 62(3): 189-90 ABSTRACT: A rare case of hereditary motor and sensory neuropathy in a 45-year-old man with glove and stocking hypoaesthesia, bilateral clawing, foot drop, and thickening of the peripheral nerves mimicking Hansen's disease is reported. KEYWORDS: Neuropathies, Hereditary Motor and Sensory/PA; Neuropathies, Hereditary Motor and Sensory/DI; Neuropathies, Hereditary Motor and Sensory/PP; Ulcer/PA; Leprosy/PA; Leprosy/DI; Leprosy, Lepromatous; Nervous System Diseases; Middle Age; Human; Male; Case Report References: 4 Record Identifier: TB3833
Entrez PubMed
Click here to read Autosomal dominant sensory/motor neuropathy with Ataxia AD) spinocerebellarataxias (SCAs) and hereditary sensory neuropathies (HSN) are
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Indian Pediatrics - Editorial
hereditary sensory and Autonomic Neuropathies (HSAN) are a group of rare disorderscharacterized by prominent sensory and autonomic neuropathy without motor
http://www.indianpediatrics.net/sep2002/sep-870-874.htm
References For Neuropathy, Hereditary Motor And Sensory, Russe
References for neuropathy, hereditary motor and sensory, Russe type withthe MeSH term Craniofacial Abnormalities, G2D Home. PMID and date.
http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Craniofacial_Abnorma
References For Neuropathy, Hereditary Motor And Sensory, Russe
References for neuropathy, hereditary motor and sensory, Russe type withthe MeSH term Demyelinating Diseases, G2D Home. PMID and date.
http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Demyelinating_Diseas
The Association Of Hereditary Spastic Paraplegia And Hereditary Motor And Sensor
In the third case (the mother of the siblings), the clinical diagnosis was consistentwith hereditary motor sensory neuropathy type 2, which was also confirmed
http://medicine.inonu.edu.tr/dergi/Contents/Volume2/Issue2/Abstract/193-195.html

Extractions: The association of hereditary spastic paraplegia and hereditary motor and sensory neuropathy in the same family Münife Müftüoðlu , M.D., Ý. Özcan Ertürk , M.D., Cemal Özcan , M.D., Hakan Ekmekçi , M.D. The association of hereditary spastic paraplegia (HSP) and sensory neuropathies have been reported in a number of cases. But it is rare to detect both entities seperately in different members of the same family. In the present study, we report clinical and electrophysiological findings of three members of a family. In two of the siblings the clinical picture was indistinguishable from "pure" hereditary spastic paraplegia, but electrophysiological studies revealed a predominantly sensory polyneuropathy. In the third case (the mother of the siblings), the clinical diagnosis was consistent with hereditary motor sensory neuropathy type 2, which was also confirmed by electrophysiological studies. We believe that, with the further genetic reevaluations, the hereditary spastic paraplegia with sensory abnormalities may take a new place in the classification of hereditary motor and sensory polyneuropathies, as a distinct entity.[Journal of Turgut Özal Medical Center 2(2):193-195,1995] Key Words : Hereditary spastic paraplegia, hereditary motor and sensory neuropathy
OUP: Diagnosis And Management Of Peripheral Nerve Disorders: Mendell
19 Diabetic Neuropathies; 20 Peripheral neuropathy Associated withHIV Infection; 21 hereditary motor and sensory Neuropathies; 22
http://www.oup.co.uk/isbn/0-19-513301-3

Extractions: VIEW BASKET Quick Links About OUP Career Opportunities Contacts Need help? oup.com Search the Catalogue Site Index American National Biography Booksellers' Information Service Children's Fiction and Poetry Children's Reference Dictionaries Dictionary of National Biography Digital Reference English Language Teaching Higher Education Textbooks Humanities International Education Unit Journals Law Medicine Music Oxford English Dictionary Reference Rights and Permissions Science School Books Social Sciences World's Classics UK and Europe Book Catalogue Help with online ordering How to order Postage Returns policy ... Table of contents Jerry R. Mendell , Professor and Chair, Department of Neurology, Ohio State University, Columbus, John T. Kissel , Professor of Neurology, Ohio State University, Columbus, and David R. Cornblath , Professor of Neurology, John Hopkins University School of Medicine
OMIM - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATI
http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214370
OUP USA: Diagnosis And Management Of Peripheral Nerve Disorders: Jerry R. Mendel
Diabetic Neuropathies. 20. Peripheral neuropathy Associated with HIV Infection.21. hereditary motor and sensory Neuropathies and Giant Axonal neuropathy. 22.
http://www.oup.com/us/catalog/general/subject/Medicine/Neurology/?view=usa&sf=to
Hereditary Motor And Sensory Neuropathy Medical Definition Of Hereditary Motor A
Definition of hereditary motor and sensory neuropathy in the MedicalDictionary and Thesaurus. hereditary motor and sensory neuropathy.
http://medical-dictionary.thefreedictionary.com/hereditary motor and sensory neu
Hereditary Motor And Sensory Neuropathy - Encyclopedia Article About Hereditary
encyclopedia article about hereditary motor and sensory neuropathy. hereditarymotor and sensory neuropathy. Word Word.
http://encyclopedia.thefreedictionary.com/hereditary motor and sensory neuropath
AAPM&R - Case No. 43, Cont
Predominantly sensory axonal polyneuropathy with some evidence of motor involvement,axonal and hereditary sensory Autonomic neuropathy IV (HSAN IV
http://www.aapmr.org/education/emgcases/emg5903e.htm

Extractions: What is a Physiatrist? Legislative, Business and Clinical Practice Issues Annual Assembly Medical Education ... EMG EMG CASE No. 59, January 2003, continued Diagnostic Impression Nerve conduction studies showed absent sural sensory nerve potentials bilaterally, with borderline right ulnar sensory nerve evoked amplitude. Borderline low tibial compound motor action potential amplitude and delay in distal latencies bilaterally are also noted. Motor nerve conduction velocities were all borderline slow. Electromyography was essentially normal. Bibliography Hilz MJ. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations. Clin Auton Res 2002 May;12 Suppl 1:I33-43. Nolano M, Crisci C, Santoro L et al. Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis. Clin Neurophysiol 2000 Sep;111(9):1596-601.
CMGS-PMP-22 - One Gene, Two Syndromes/19.11.98
Also described as hereditary and motor sensory neuropathy (HMSN). 1. hereditary motorand sensory neuropathies, (HMSN). 2. hereditary motor neuropathies, (HMN).
http://www.ich.ucl.ac.uk/cmgs/pmp22.htm

Extractions: Keywords: CMT1A, HNPP, duplication, deletion, gene dosage First described in 1886 by Charcot and Marie in Paris, France and Tooth in Cambridge, England. Most common inherited disorder of the peripheral nerves affecting 1 in 2500 individuals in their 20s and 30s. Characterised by distal muscle atrophy and weakness, first involving the legs and particularly the peritoneal muscles. Sensory loss may be present but is always less pronounced than muscle weakness, and tendon reflexes are absent or diminished. High arched feet (pes cavus) are often present. Also described as Hereditary and Motor Sensory Neuropathy (HMSN). Studies of several cohorts of CMT patients elucidated the association between clinical phenotypes, modes of inheritance electrophysiological findings and pathological features. Extended pedigrees showed that these phenotypes bred true in families. Several subtypes of inherited peripheral neuropathies were delineated and classified as:
Neuropathy, Hereditary Sensory, Type II
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
http://www.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.
THE MERCK MANUALSECOND HOME EDITION, Hereditary Neuropathies In
hereditary neuropathies may affect only motor nerves (motor neuropathies), only sensorynerves (sensory neuropathies), or both sensory and motor nerves (sensory
http://www.merck.com/mrkshared/mmanual_home2/sec06/ch095/ch095i.jsp

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