1. Hereditary Sensory Motor Neuropathy Questions Subject hereditary sensory motor neuropathy Questions Topic Area Autonomic ForumThe Neurology and Neurosurgery Forum Question Posted By Maureen on Saturday http://www.medhelp.org/forums/neuro/archive/540.html

Questions in The Neurology Forum are being answered by doctors from The Cleveland Clinic , consistently ranked one of the best hospitals in America. Subject: Hereditary Sensory Motor Neuropathy Questions Topic Area: Autonomic Forum: The Neurology and Neurosurgery Forum Question Posted By: Maureen on Saturday, May 31, 1997 Posted by ccfNeuro MD on June 04, 1997 at 14:51:25: In Reply to: Hereditary Sensory Motor Neuropathy Questions posted by Maureen on May 31, 1997 at 09:49:35: : I have an HSMN called HNPP (Hereditary neuropathy with liability to pressure palsies). It is a relatively rare demeliniatng neuropathy and the nerves are described as tomaculous. Entrapment is typical (carpal and cubital tunnel, thoracic outlet and the evquivalent syndromses in the legs). A distinguishing feature is numbess/weakness which lasts fro minutes to months caused byu situations which would not cause problems in a "normal" person. One needs to learn to avoid situations that cause symptoms. There is no treatment. I have had symptoms for more than 15 years and have led a fairly normal life up until a couple of years ago. There had been periods where symptoms werre better and worse. Therre was a very slow progression where it took less to cause symptoms.

2. Charcot-Marie-Tooth,CMT,Hereditary Sensory Motor Neuropathy,HSMN,Peroneal Muscul CharcotMarie-Tooth,CMT,hereditary sensory motor neuropathy,HSMN,PeronealMuscular Atrophy. Charcot-Marie-Tooth http://www.icomm.ca/geneinfo/cmt.htm

Charcot-Marie-Tooth,CMT,Hereditary Sensory Motor Neuropathy,HSMN,Peroneal Muscular Atrophy,Charcot-Marie-Tooth,CMT,Hereditary Sensory Motor Neuropathy,HSMN,Peroneal Muscular Atrophy For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Charcot-Marie-Tooth also known as: CMT Peroneal Muscular Atrophy Hereditary Sensory Motor Neuropathy HSMN (as defined by the National Organization for Rare Disorders Charcot-Marie-Tooth disease is a hereditary neurological disorder characterized by muscle weakness and atrophy, primarily in the legs. Disappearance of the protective fatty layers surrounding the nerves (segmental demyelination) of peripheral nervous system and associated degeneration of part of the nerve cells (axons) characterize this disorder. (as defined by the National Institute for Neurological Disorders and Strokes NINDS Charcot-Marie-Tooth Disorder Information Page Reviewed 09-05-2001 What is Charcot-Marie-Tooth Disorder?

3. Neuropathy Hereditary Sensory Type I,Acrodystrophic Neuropathy,Hereditary Sensor Called also hereditary sensory and motor n. http//www.medhelp.org/forums/neuro/archive/540.htmlSubject hereditary sensory motor neuropathy Questions Topic http://www.icomm.ca/geneinfo/hsn.htm

Hereditary Sensory Neuropathy The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Hereditary Sensory Neuropathy also known as: 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 Hereditary Sensory Neuropathy type I Hereditary Sensory Neuropathy type II (as defined by the National Organization for Rare Disorders Hereditary Sensory Neuropathy type I 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. Hereditary Sensory Neuropathies of various types may attack a single nerve (mononeuropathy, mononeuritis), or several nerves in asymmetric areas of the body (mononeuritis multiplex), or many nerves simultaneously (polyneuropathy, polyneuritis, multiple peripheral neuritis).

4. Charcot Marie Tooth Disease report. Synonyms CMT; hereditary sensory motor neuropathy; HSMN; PeronealMuscular Atrophy. Disorder Subdivisions None. General Discussion http://my.webmd.com/hw/health_guide_atoz/nord261.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 Charcot Marie Tooth Disease Important It is possible that the main title of the report Charcot Marie Tooth Disease 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 CMT Hereditary Sensory Motor Neuropathy HSMN Peroneal Muscular Atrophy Disorder Subdivisions None General Discussion Charcot-Marie-Tooth disease is a hereditary neurological disorder characterized by muscle weakness and atrophy, primarily in the legs. Disappearance of the protective fatty layers surrounding the nerves (segmental demyelination) of peripheral nervous system and associated degeneration of part of the nerve cells (axons) characterize this disorder. Resources Charcot-Marie-Tooth Association 2700 Chestnut St Chester, PA 19013

5. Charcot Marie Tooth Disease Synonyms. CMT; hereditary sensory motor neuropathy; HSMN; PeronealMuscular Atrophy. Disorder Subdivisions. None. Related Disorders List. http://www.bchealthguide.org/kbase/nord/nord261.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord261"; var hwDocTitle="Charcot Marie Tooth Disease"; var hwRank="1"; var hwSectionHWID="nord261"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Charcot Marie Tooth Disease 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 CMT Hereditary Sensory Motor Neuropathy HSMN Peroneal Muscular Atrophy Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Dejerine-Sottas Disease Hereditary Sensory Radicular Neuropathy Refsum Syndrome Familial Amyloid Neuropathy Hereditary Neuropathy with Liability to Pressure Palsy (HNPP) General Discussion Charcot-Marie-Tooth disease is a hereditary neurological disorder characterized by muscle weakness and atrophy, primarily in the legs. Disappearance of the protective fatty layers surrounding the nerves (segmental demyelination) of peripheral nervous system and associated degeneration of part of the nerve cells (axons) characterize this disorder. Symptoms Symptoms of Charcot-Marie-Tooth disease usually begin gradually sometime between middle childhood and age 30. Muscle atrophy and weakness are most prominent in the legs and the small muscles of the hands. The most incapacitating symptom of CMT is "foot drop", producing a slapping gait. Pain and unusual sensations (paresthesias) may be present in the affected limbs. A decrease in vibration, pain and thermal sensation in the hand, foot and lower part of the leg (glove and stocking pattern) is common. Stretch reflexes are usually absent. The disease is slowly progressive, but may arrest spontaneously. Patients may remain active for years and live a normal life span.

6. G Therapy - Case Studies Case No 5 hereditary sensory motor neuropathy Axonal Demyelinating.Omkar Shetye is a 8 Years old boy with hereditary sensori http://www.g-therapy.org/neurologycs5.htm

Home Contact Us *Volunteers/Researchers* Welcome to Neuropathy Research Section Range of Ayurvedic Oils. Omkar Shetye is a 8 Years old boy with hereditary sensori – motor neuropathy with deafness and has one elder sister who is very similarly affected. He was seen at our center in Nov’98 and started on Neuro G-Therapy. One month after therapy few NCV improvements were noted. On Examination: Head circumference 50.5 cm. Marked squint both eyes. No abnormal facies or dermo - glyphics. Pes planus, feet are narrow and small, 3rd toe of both feet hypotrophic. Scratch marks and injuries all over lower limb and upper limb- suggesting a sensory component. CNS Examination : Alert Cooperative. Smiles, imitates action. Understanding/ Intelligence is fair if due concessions are made for his deafness and no special training. Investigations Before Neuro G-Therapy : November 1994 : Diffuse sensory neuropathy.

7. Disease - Charcot-Marie-Tooth Disease (CMT) SearchTerm, hereditary sensory motor neuropathy (HSMN), Peroneal muscularatrophy (PMA), Neuropathy with focally folded myelin sheaths, Congenital http://www.rehabinfo.net/resources/diseases/list/disease.asp?id=5

8. Diagnosis Case 15 The differential diagnosis of the peripheral neuropathy presented in this case includesa form of hereditary sensory motor neuropathy (HMSN), vasculitis, and http://sprojects.mmi.mcgill.ca/neuropath/case15/15diag.htm

Final Diagnosis Tomaculous Neuropathy Clinical discussion: Physical examination in HNPP often reveals weakness and sensory loss attributable to a specific nerve distribution. However, if the disease is advanced and many nerves are affected, findings may be generalized as in the patient above, thereby mimicking a distal sensorimotor peripheral neuropathy, such as CMT-I. The symptoms would then include a decrease in distal limb reflexes, weakness and wasting of the intrinsic muscles of the hand and foot, and a decreased vibration sense. The nerve conduction studies in HNPP usually show a widespread polyneuropathy. Motor and sensory conduction abnormalities are found not only in affected nerves, but also in those that are clinically normal. Unaffected nerves show prolongation of distal latency, mild slowing of conduction velocities, and reduced amplitude. Affected nerves show segmental slowing or block, especially at entrapment sites. There is a decrease in amplitude of the compound muscle action potential when the nerve is stimulated proximal to the block. Needle EMG studies are normal in clinically unaffected nerves. In mild cases, the EMG shows a reduction in voluntarily activated motor unit potentials. In severe cases, signs of active denervation such as increased insertional activity or fibrillation potentials are more prominent. Microscopy discussion The muscle biopsy of this patient demonstrated a number of features consistent with a denervation-reinnervation process: variation in muscle fiber size, large sheets of smaller diameter fibers, and fiber-type grouping. The nerve biopsy showed a shift to smaller diameter nerve fibers, which corresponds to the slowed velocities seen on nerve conduction studies. As is characteristic in HNPP, both affected and unaffected nerves of the patient showed areas of myelin thickening (tomaculae) that are particularly convincing in the teased nerve fiber preparations.

9. Medicdirect - Comprehensive UK Health Information Some forms of chronic neuropathy that are predominantly motor are familial.These are known as hereditary sensory motor neuropathy (HSMN). http://www.medicdirect.co.uk/clinics/default.ihtml?step=4&pid=769

10. Dominantly Inherited Peripheral Neuropathies Keywords CharcotMarie-Tooth, hereditary sensory motor neuropathy, Peripheral neuropathy.© Copyright by American Association of Neuropathologists, Inc. 2003. http://apt.allenpress.com/aptonline/?request=get-abstract&issn=0022-3069&volume=

11. ICON Health Publications -- Index Hereditary Motor Sensory Neuropathy. Hereditary Motor Sensory NeuropathyI. hereditary sensory motor neuropathy. Hereditary Spastic Paraplegia. http://www.icongrouponline.com/browse/Health/healthH.html

ICON Group Browse - Health Health Publications A B C D ... Webster's Online Dictionary - The Rosetta Edition.

12. Charcot-Marie-Tooth Disorder Sensory Neuropathy; Hereditary Motor Sensory Neuropathy I; Hereditary peroneal nervedysfunction; hereditary sensory motor neuropathy; Idiopathic dominantly http://www.icongrouponline.com/health/Charcot-Marie-Tooth.html

ICON Health Publications Official Health Sourcebooks The Official Patient's Sourcebook on CHARCOT-MARIE-TOOTH DISORDER (Charcot-Marie-Tooth Disease (Variant); Charcot-Marie-Tooth-Roussy-Levy Disease; Hereditary Areflexic Dystasia; Hereditary Motor and Sensory Neuropathy; Hereditary motor and sensory neu-ropathy; Hereditary Motor Sensory Neuropathy; Hereditary Motor Sensory Neuropathy I; Hereditary peroneal nerve dysfunction; Hereditary Sensory Motor Neuropathy; Idiopathic dominantly inherited hy-pertrophic polyneuropathy; Neuropathy - peroneal (hereditary); peroneal muscular atrophy; Progressive neuropathic (peroneal) muscular atrophy) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Electronic File *E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Charcot-Marie-Tooth. Fully referenced with ample Internet listings and glossary.

13. Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Hereditary+Motor+and+Sensory+Neuropathie ADC Mercuri et al. 81 (5) 442 Neurophysiological and genetic analysis at age 8 years indicated that vincristinehad induced symptoms of a hereditary sensory motor neuropathy type 1A, which http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Hereditary Motor and Sensory Neur

14. HSN hereditary sensory motor neuropathy with Ulceromutilation Dominant;sensory motor; hereditary sensory-motor neuropathy with http://www.neuro.wustl.edu/neuromuscular/time/hsn.htm

Front Search Index Links ... Patient Info HSN Disorder Gene Chromosome Inheritance Clinical features Cajal I Dominant Small axon loss Acromutilation II Recessive III IKBKAP Recessive Riley-Day Syndrome IV TRKA/ NGF receptor Recessive Congenital sensory neuropathy with anhidrosis C-axon loss V Recessive Congenital absence of pain No anhidrosis Absent pain NGF- b Recessive Absence of pain No anhidrosis Biemond congenital anaesthesia Dominant Large fiber sensory loss Ataxic neuropathy Dominant Large fiber sensory loss Ataxia Ulcero-mutilation Dominant Acromutilation Hereditary sensory neuropathy with (Tangier's) Anosmia Ataxia telangectasia Friedreich's ataxia Mitochondrial disorder Maternal: NARP Recessive: Cytopathy Multiple symmetrical lipomatosis Posterior column ataxia + Retinitis pigmentosa ... Spastic paraparesis Hereditary Neuropathies with Ulcero-mutilation HSAN I : Dominant; Sensory HMSN 2B : Dominant; Sensory + Motor Hereditary Sensory-Motor Neuropathy with Ulcero-mutilation Recessive axonal CMT with acrodystrophy Also see Occasional patients with CMT 1A Neurogenic osteoarthropathies (Charcot's joints) Animal model: mutilated foot rat l desert hedgehog (DHH) ; Chromosome 12q12-q13.1; Sporadic (Recessive)

15. Hereditary Motor Sensory Neuropathies: Charcot-Marie-Tooth hereditary motor sensory NEUROPATHIES (HMSN; CMT). HMSNP CMT 2-P 0 hereditarysensory-motor neuropathy with Ataxia 26 l Chromosome 7q22-q32; Dominant 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 CMT 1E : P protein; 1q22 CMT 1F : Neurofilament light chain; 8p21 HNPP : PMP-22 deletion; 17p11 HMSN 3 (Dejerine-Sottas) PMP-22; P Thermosensitive Sensory PN + hearing loss : Connexin-31; 1p35 Hypomyelin, No symptoms 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 : Ceramidase; 8p22 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 Pyramidal signs Axonal Dominant CMT 2A CMT 2A CMT 2B CMT 2C ... CMT 2D : GARS; 7p14 CMT 2E : Neurofilament light chain; 8p21 CMT 2F CMT 2G CMT 2I : P CMT 2J : P CMT 2L HMSN-Proximal HMSN 5 : Pyramidal signs HMSN 6 HMSN + Optic atrophy HMSN + Deafness HSMN + Ulcero-mutilation ... AR-CMT2A : Lamin A/C; 1q21

16. Hereditary Sensory-motor Neuropathy Type 7 Information Diseases Database hereditary sensorymotor neuropathy type 7 Information 3 synonyms or equivalents were found. hereditary sensory-motor neuropathy type 7 http://www.diseasesdatabase.com/ddb32094.htm

Diseases Database Index Sponsors Contact ... Previous Page Hereditary sensory-motor neuropathy type 7 Information Search 3 synonyms or equivalents were found. Hereditary sensory-motor neuropathy type 7 aka/or HSMN type 7 aka/or Hereditary sensorimotor neuropathy type 7 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 7: specific sites Send Hereditary sensory-motor neuropathy type 7 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 22:13:40 Metadata Updated 2004-05-22

17. 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: 05/27/04

18. EMedicine - Charcot-Marie-Tooth And Other Hereditary Motor And Sensory Neuropath 1893). More recent nomenclature designated CharcotMarie-Tooth diseaseas a hereditary motor and sensory neuropathy (HMSN). Recent http://www.emedicine.com/neuro/topic468.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Neurology Neuromuscular Diseases Charcot-Marie-Tooth and Other Hereditary Motor and Sensory Neuropathies Last Updated: January 16, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: Charcot-Marie-Tooth, Charcot-Marie-Tooth neuropathy, Charcot-Marie-Tooth disorder, Charcot-Marie-Tooth neuromuscular disease, Charcot-Marie-Tooth neurologic disease, Charcot-Marie-Tooth syndrome, 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 AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Aamir Hashmat, MD

19. AAEM - Patient Resources - Hereditary Motor Sensory Neuropathy Patient Resources hereditary motor sensory neuropathy. Membership Directory. Practice Issues / Advocacy. Employment/Training. Career Center. Fellowship Listing. EDX Courses. Training Links. Training Program/ In-Service Exam. News. Contact the Staff List Rental. hereditary motor sensory neuropathy (HMSN/Charcot-Marie-Tooth disease 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

20. Hereditary Sensory-motor Neuropathy Type 6 Information Diseases Database hereditary sensorymotor neuropathy type 6 Information 3 synonyms or equivalents were found. hereditary sensory-motor neuropathy type 6 http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=32095

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