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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

1. Welcome To CMT United Kingdom
   CMT United Kingdom, the UK support group for people affected by CharcotMarie-Tooth disease, also known as Hereditary Motor Sensory Neuropathy and  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

2. Clinical Neurosciences - Hereditary Motor And Sensory Neuropathy
   HEREDITARY MOTOR SENSORY NEUROPATHY (HMSN)  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

3. Hereditary Sensory Motor Neuropathy Questions
   Patient medical question and doctor answer from The Neurology and Neurosurgery Forum. Health topic area and articles about autonomic Topics peripheral .  
   http://www.medhelp.org/forums/neuro/archive/540.html
   
   Extractions: : 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. A few years ago, I had a traumatic injury to one nerve, causing mostly pain, and that seemed to set the neuopathy off into a fasirly rapid decline. I have pain, numbness and motor problems (foot drop, difficulty writing, dropping things, etc) , in all 4 limbs, which seems to vary in intensity day to day. It's getting harder to walk and climb stairs. And while having sensations of numbness, I also have an exaggerated response to pin pricks, etc.

4. Muscular Dystrophy Association Diseases -Charcot-Marie-Tooth
   CharcotMarie-Tooth Disease (CMT) (Also known as Hereditary Motor and Sensory Neuropathy (HMSN) or Peroneal Muscular Atrophy (PMA))  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

5. Facts About Rare Muscular Dystrophies
   Because of these features, CMT is sometimes called hereditary and motor sensory neuropathy (HMSN). Some doctors also use the old  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

6. Hereditary Motor Sensory Neuropathies Charcot-Marie-Tooth
   HEREDITARY MOTOR SENSORY NEUROPATHIES (HMSN; CMT) CMT HMSN Demyelinating Dominant CMT 1A PMP22; Demyelinating neuropathy. Intermediate  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

7. Charcot Marie Tooth Disease
   CMT; hereditary sensory motor neuropathy; HSMN; Peroneal Muscular Atrophy. Disorder Subdivisions. None. General Discussion. Charcot Marie Tooth hereditary  
   http://my.webmd.com/hw/brain_nervous_system/nord261.asp
   
   Extractions: Charcot Marie Tooth hereditary neuropathies are a group of disorders in which the motor and sensory peripheral nerves are affected, resulting in muscle weakness and atrophy, primarily in the legs and sometimes in the hands. CMT hereditary neuropathy affects the nerves that control many muscles in the body. The nerve cells in individuals with this disorder are not able to send electrical signals properly because of abnormalities in the nerve axon or abnormalities in the insulation (myelin) around the axon. Specific gene mutations are responsible for the abnormal function of the peripheral nerves. Charcot Marie Tooth hereditary neuropathy can be inherited in an autosomal dominant, autosomal recessive or X-linked mode of inheritance. Resources

8. Welcome To The Charcot-Marie-Tooth Association
   Become a Member of the CMTA!  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. CMT Charcot-Marie-Tooth HMSN Hereditary Motor Sensory Neuropathy
   Tooth Disease (CMT) is the most common Hereditary Neuromuscular Disease known. It is also known as "Hereditary MotorSensory Neuropathy" (HMSN  
   http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. Roussy-Levy Syndrome Charcot-Marie-Tooth Disease
    ToothRoussy-Levy Disease Hereditary Areflexic Dystasia Hereditary Motor Sensory Neuropathy Hereditary Motor Sensory Neuropathy I  
    http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

11. Autosomal Recessive Hereditary Motor And Sensory Neuropathy With
    Autosomal Recessive Hereditary Motor and Sensory Neuropathy with Focally Folded Myelin Sheaths (CMT4B) ANTONIO GAMBARDELLAa b  
    http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

12. BOFFS - Development Of Charcot Joint Following Surgery In Hereditary Sensory Mot
    Development of Charcot joint following surgery in hereditary sensory motor neuropathy (CharcotMarie-Tooth disease). *M. Nyska MD, **M. Myerson MD  
    http://www.bofss.org.uk/html/development_of_charcot_joint_following_surgery_in_h
    
    Extractions: 1999 abstracts Outcome of tarsometatarsal arthrodesis Wound healing following partial closure of the Cincinnati incision for surgery of congenital talipes equinovarus Does addition of footblock for daycase foot surger ... Subtalar distraction fusion after calcaneal fractures using RAMP cage Development of Charcot joint following surgery in hereditary sensory motor neuropathy (Charcot-Marie-Tooth disease) *M. Nyska M.D., **M. Myerson M.D. Charcot-Marie-Tooth (CMT) disease is a spectrum of peripheral neuropathy affecting motor and sensory nerves of the extremity. Most of these patients manifest with progressive distal weakness, pes cavovarus and family history. In advanced cases surgical treatment to correct the foot deformity tendon transfers, soft tissue release, osteotomies, and arthrodesis is needed. Destructive joint process compatible with Charcot changes may rarely appear, mainly in weight bearing joints. The mechanism responsible for activation of the Charcot process is not known but has been associated with neuropathy and fractures in diabetics. We present 3 cases having CMT who developed Charcot destructive process of ankles in two patients and midfoot in another patient. The process developed during recovery period for reconstructive surgery and may have been the trigger for initiating the process. The possible mechanism for development of Charcot process in these patients are discussed.

13. Arch Neurol Abstract Hereditary Motor And Sensory Neuropathy
    Topic Collection Alerts Hereditary Motor and Sensory Neuropathy Type 2C Is Genetically Distinct From Types 2B and 2D Masaaki Nagamatsu, MD  
    http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. Charcot Marie Tooth Disease
    Charcot Marie Tooth hereditary neuropathies are a group of disorders in which CMT; hereditary sensory motor neuropathy; HSMN; Peroneal Muscular Atrophy  
    http://www.bchealthguide.org/kbase/nord/nord261.htm
    
    Extractions: 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. Charcot Marie Tooth hereditary neuropathies are a group of disorders in which the motor and sensory peripheral nerves are affected, resulting in muscle weakness and atrophy, primarily in the legs and sometimes in the hands. CMT hereditary neuropathy affects the nerves that control many muscles in the body. The nerve cells in individuals with this disorder are not able to send electrical signals properly because of abnormalities in the nerve axon or abnormalities in the insulation (myelin) around the axon. Specific gene mutations are responsible for the abnormal function of the peripheral nerves. Charcot Marie Tooth hereditary neuropathy can be inherited in an autosomal dominant, autosomal recessive or X-linked mode of inheritance. Charcot-Marie-Tooth Association

15. Hill Health Topics A-Z - Charcot Marie Tooth Disease
    CMT; hereditary sensory motor neuropathy; HSMN; Peroneal Muscular Atrophy Charcot Marie Tooth hereditary neuropathy can be inherited in an autosomal  
    http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord261&SE

16. Medicdirect - Comprehensive UK Health Information
    These are known as hereditary sensory motor neuropathy (HSMN). These can be suspected clinically and neurophysiological tests can be supportive but in  
    http://www.medicdirect.co.uk/diseases/default.ihtml?pid=769&step=4

17. Journal Of Clinical Neuromuscular Disease - UserLogin
    Precipitation of Hereditary MotorSensory Neuropathy Following Hepatitis B hereditary sensory motor neuropathy degenerative disease or a disease with  
    http://www.jcnmd.com/pt/re/jclnnmd/fulltext.00131402-200112000-00005.htm

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

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

20. Charcot-Marie-Tooth Disorder
    Hereditary Motor Sensory Neuropathy I; Hereditary peroneal nerve dysfunction; hereditary sensory motor neuropathy; Idiopathic dominantly inherited  
    http://www.icongrouponline.com/health/Charcot-Marie-Tooth.html
    
    Extractions: (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 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. Related Conditions/Synonyms 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

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