41. Hereditary Motor And Sensory Neuropathies (HMSN, CMT) of disorders is known as hereditary motor and sensory neuropathies (HMSN) and CharcotMarie-Tooth (CMT1A) / hereditary motor and sensory neuropathy http://www.muscle.ca/content/index.php?id=150

42. Hereditary Motor And Sensory Neuropathy With Agenesis Of The Corpus Callosum This brochure on hereditary motor and sensory neuropathy with Agenesis of the What is hereditary motor and sensory neuropathy with Agenesis of the http://www.muscle.ca/content/index.php?id=998

43. Headache Most neuropathies affect both sensory and motor; Pure motor or sensory seen in Toxin exposure; Vitamin B12 Deficiency; hereditary sensory neuropathy http://www.fpnotebook.com/NEU255.htm

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44. Research Reports- Hereditary Motor Sensory Neuropathy The hereditary neuropathies include hereditary motor sensory neuropathy (HMSN), hereditary motor neuropathy and hereditary sensory and autonomic neuropathy, http://disability.ucdavis.edu/rrtc/publications/research_summaries/Hereditary_mo

NIDRR Rehabilitation Research and Training Center in Neuromuscular Diseases (RRTC/NMD) Search Site Path: Home rrtc publications Hereditary_mo.asp September 8, 2005 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.

45. Peripheral Neuropathy However, segmental demyelination can also occur in some hereditary A host of symptoms and signs that reflect sensory, motor, and autonomic nerve fiber http://www.clevelandclinicmeded.com/diseasemanagement/neurology/pneuro/pneuro.ht

Published February 9, 2004 Robert W. Shields, Jr, MD Department of Neurology Print Chapter The Cleveland Clinic Foundation The peripheral nervous system can be involved in a wide range of medical disorders with various pathophysiologies (Table 1) It may be affected by numerous toxins, both drugs (Table 2) and industrial agents (Table 3) chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), and multifocal motor neuropathy with conduction block syndrome (MMNCB). Finally, a host of hereditary polyneuropathies may cause a wide range of peripheral neuropathy syndromes (Table 4) This diverse array of possible etiologies can make the diagnosis of peripheral neuropathies quite challenging. Nevertheless, diagnosis can be facilitated with a systematic approach that classifies the peripheral neuropathy on the basis of clinical features, taking into account the type of peripheral nerve fiber that may be involved ( ie, sensory, motor, or autonomic), the distribution or pattern of peripheral nerve-fiber involvement (ie, generalized and symmetric versus asymmetric and multifocal), and lastly, the mode of evolution (ie, acute, subacute, or chronic). Definition Prevalence Pathophysiology Signs and ... References DEFINITION Peripheral neuropathy, in the broadest sense, refers to a scope of clinical syndromes

46. Peripheral Neuropathy -- Printable Tables Acute motor and sensory axonal neuropathy syndrome hereditary sensory and autonomic neuropathy types I, III, IV; Fabry s disease; Tangier disease http://www.clevelandclinicmeded.com/diseasemanagement/neurology/pneuro/pneurotab

TITLE: PERIPHERAL NEUROPATHY AUTHORS: ROBERT W. SHIELDS MD Department of Neurology PUBLISHED: FEBRUARY 9, 2004 Table 1: Peripheral Neuropathy Syndromes I. Acute-Subacute Generalized Polyneuropathies A. Sensorimotor 1. Acute motor and sensory axonal neuropathy syndrome 2. Alcohol/nutritional 3. Toxins (metals) 1. Guillain-Barre syndrome 2. Acute motor axonal neuropathy syndrome 3. Porphyria 4. Diphtheria 5. Toxins (dapsone, vincristine) C. Sensory 1. Paraneoplastic/autoimmune (anti-Hu associated) 2. Vitamin B toxicity 3. Toxins (cisplatin) 4. Human immunodeficiency virus II. Chronic Generalized Symmetric Polyneuropathies A. Sensorimotor 1. Diabetes 2. Uremia 3. Alcohol/nutritional 4. Dysproteinemias 5. Connective tissue diseases

47. Charcot-Marie-Tooth Disease - MayoClinic.com signs and symptoms, severity, and progression. Other names for CMT include hereditary motor and sensory neuropathy and peroneal muscular atrophy. http://www.mayoclinic.com/invoke.cfm?id=DS00557

48. Netter Medical Artwork - Hereditary Motor-Sensory Neuropathy Type III - Image 11 Title, hereditary motorsensory neuropathy Type III. Image , 1172 hereditary eye diseases hereditary motor sensory neuropathy Heredodegenerative http://www.netterimages.com/image/detail.htm?variantID=1172

49. Hereditary Sensory And Autonomic Neuropathy (HSAN) Pediatric Oncall Thus, she was diagnosed as a case of hereditary sensory neuropathy. motor nerve conduction velocities are normal, but the sensory nerve action http://www.pediatriconcall.com/fordoctor/casereports/hsan.asp

DOCTOR CORNER Search GO Home Back Ask Doctor Post Query Education Image Gallery Teaching Files Question of the day Specialist Answers Latest Updates Conference Journal Search Original Articles Clinical Trials Search For Pediatricians Hospitals Special Schools Drug Index ... Sign Out HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY (HSAN) UserName Password New Register Forgot password Dr. Ira Shah M.D, DNB, DCH(Gold Medalist), FCPS Case Report : A 5 year old female child, 3rd of 3 siblings born of third degree consanguineous marriage presented with intermittent fever since birth, self mutilation since 2½ years of age and ulcer over left middle toe with blackening since 10-12 days. Other 2 elder siblings had died (one due to fever at 2 months and second at 3 months due to altered sensorium). She was immunized till date, however there was no history of crying on receiving injections. She had multiple ulcers in the past and she required amputation of the left great toe due to gangrene at the age of 4½ years. Her milestones were delayed. At present she was able to only speak bisyllables and walk without support. On examination, there was an ulcer over the left second toe and she had absent left great toe. She had bitten off the distal phalynx of the right index finger (Figure 1). < 79 suggestive of mild mental delay. Thus, she was diagnosed as a case of Hereditary sensory neuropathy.

50. Neuropathy Hereditary Motor And Sensory, Lom Type Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/GB/neuropathy_hereditary_motor_and_sensory.html

51. Arch Ophthalmol -- Hereditary Motor And Sensory Neuropathy Associated With Juven hereditary motor and sensory neuropathy (HMSN) belongs to a heterogeneous group of hereditary neurological disorders characterized by progressive muscular http://archopht.ama-assn.org/cgi/content/extract/119/10/1547

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 119 No. 10, October 2001 Featured Link E-mail Alerts Clinicopathologic Reports, Case Reports, and Small Case Series Article Options Full text PDF Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Unoki K Osame M ISI Web of Science (2) Contact me when this article is cited Hereditary Motor and Sensory Neuropathy Associated With Juvenile Glaucoma Arch Ophthalmol. Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. INTRODUCTION Hereditary motor and sensory neuropathy (HMSN) belongs to a heterogeneous group of hereditary neurological disorders characterized by progressive muscular atrophy and weakness of limbs due to peripheral neuropathies or Charcot-Marie-Tooth disease (CMT)

52. Analysis Of Neuropathy, Hereditary Motor And Sensory, Russe Type Disease mapped neuropathy, hereditary motor and sensory, Russe type Chromosome 10 neuropathy tw AND motor tw AND sensory tw AND Lom tw http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U59333

53. Analysis Of Neuropathy, Hereditary Motor And Sensory, Okinawa Type Disease mapped neuropathy, hereditary motor and sensory, Okinawa type Chromosome 3 neuropathy tw AND motor tw AND sensory tw AND Okinawa tw http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U50989

54. V, HMSN (Hereditary Motor And Sensory Neuropathy Type V) : On Medical Dictionary V, HMSN (hereditary motor and sensory neuropathy Type V) defined on the Free Online Medical Dictionary. Medical terminology definitions including drugs, http://www.online-medical-dictionary.org/V, HMSN (Hereditary Motor and Sensory N

55. Current Concepts In The Diagnosis And Treatment Of Peripheral Neuropathies hereditary motor and sensory neuropathy (HMSN) or Charcot Marie Tooth disease (CMT) is a heterogeneous group of disorders. http://www.dcmsonline.org/jax-medicine/2000journals/august2000/neuropathies.htm

Current Concepts In The Diagnosis And Treatment Of Peripheral Neuropathies Alan R. Berger, M.D. and Michael Pulley, M.D., PhD. Alan R. Berger, M.D. is Professor of Neurology, University of Florida Health Science Center/Jacksonville and Chairman, Department of Neurology, Shands Jacksonville. Michael Pulley, M.D., Ph.D. is Assistant Professor of Neurology, University of Florida Health Science Center/Jacksonville and Director, EMG Laboratory, Shands Jacksonville. Decisions regarding whom, when, and how to treat depend not only on the underlying etiology, but the nature of the clinical deficits, their severity and rate of progression, and the overall medical condition of the patient. In addition to administering specific treatment aimed at retarding the progression or resolving the neuropathy, care should also be directed to pain management, orthotics, and improving gait stability. This article will briefly discuss the clinical description, laboratory features, and treatment options of a select group of PNs most likely to be encountered in routine clinical practice. The reader is referred to the references for more detailed descriptions of these and other PNs. Immune Mediated Neuropathies Guillain-Barré Syndrome Guillain-Barré syndrome (GBS) The underlying pathology often determines the clinical severity and course. Improvement tends to be more rapid and complete in those cases with greater demyelinating than axonal pathology. GBS occurs at any age and has an annual incidence of 1-2/100,000. Two-thirds of patients have a premonitory illness, usually viral (cytomegalovirus, Epstein Barr virus, and HIV are most common). Myocplasma pneumoniae and Camplybacter jejuni are the most common non-viral pathogens. Documenting the nature of the preceding illness usually has little clinical value, except when GBS heralds HIV infection.

56. 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: 06/09/04

57. Neuropathy, Hereditary Sensory, Type I - St. Joseph Mercy, Ann Arbor Michigan hereditary sensory neuropathy Type I (HSN I) is a rare genetic disorder characterized These symptoms may involve sensory, motor, reflex, or blood vessel http://www.sjmercyhealth.org/14775.cfm

@import url(default.css); Online Health Information Health Information - Rare Diseases and Disorders Back to Health Library Print This Page Email to a Friend National Organization for Rare Disorders, Inc. Neuropathy, Hereditary Sensory, Type I Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Neuropathy, Hereditary Sensory, Type I 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 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 None General Discussion 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). These symptoms may involve sensory, motor, reflex, or blood vessel (vasomotor) functions.

58. Penn State Faculty Research Expertise Database (FRED) hereditary, Type III, motor and sensory neuropathy, hereditary, Type VII, motor and Neuropathies, hereditary motor and sensory, Dejerine Sottas Disease http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D015417

59. American Family Physician: An Algorithm For The Evaluation Of Peripheral Neuropa Peripheral neuropathy has numerous other causes, including hereditary, toxic, Large, myelinated axons include motor axons and the sensory axons http://www.findarticles.com/p/articles/mi_m3225/is_n4_v57/ai_20383463

@import url(/css/us/style1.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); @import url(/css/us/artHome1.css); Advanced Search Home Help IN free articles only all articles this publication Automotive Sports 10,000,000 articles - not found on any other search engine. FindArticles American Family Physician Feb 15, 1998 Content provided in partnership with 10,000,000 articles Not found on any other search engine. Featured Titles for AAACN Viewpoint ABNF Journal, The AIDS Treatment News AMAA Journal ... View all titles in this topic Hot New Articles by Topic Automotive Sports Top Articles Ever by Topic Automotive Sports An algorithm for the evaluation of peripheral neuropathy American Family Physician Feb 15, 1998 by Ann Noelle Poncelet Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. The incidence of peripheral neuropathy is not known, but it is a common feature of many systemic diseases. Diabetes and alcoholism are the most common etiologies of peripheral neuropathy in adults living in developed countries. The primary worldwide cause of treatable neuropathy is leprosy.[1] Neuropathies associated with human immunodeficiency virus (HIV) infection account for an increasing number of cases. Peripheral neuropathy has numerous other causes, including hereditary, toxic, metabolic, infectious, inflammatory, ischemic and paraneoplastic disorders. The number of peripheral neuropathies for which an etiology cannot be found despite extensive evaluation ranges from 13 to 22 percent.[2,3] Many undiagnosed patients (up to 42 percent) are found, after a careful family history and examination of kin, to have a familial neuropathy.[2]

60. Hereditary Recurrent Neuropathies Among hereditary neuropathies a sub group is characterized by recurrent focal of cases sensory neuropathy , sensorymotor neuropathy mimicking CMT http://www.charite.de/ch/medgen/eumedis/neurogenetics05/hereditary-rec-neuropath

Home Up Up topic About Clinical and genetic aspect of autosomal dominant cerebellar ataxia type II (ADCA II) Autosomal dominant cerebellar ataxias Physiopathological aspects of spinocerebellar ataxias ... Dominant forms of Charcot-Marie-Tooth diseases Hereditary Recurrent Neuropathies Clinical and Genetic Aspects of Dystrophinopathies The Sarcoglycanopathies Nuclear factor-KappaB (NF-κB) in dystrophinopathies Gene expression profile investigation of acquired muscle disorders ... Glycogen Storage Myopathies: from clinical features to treatment Font size: Hereditary Recurrent Neuropathies Riadh Gouider Abstract Among hereditary neuropathies a sub group is characterized by recurrent focal peripheral nerve lesions with acute or subacute onset. It includes: Herditary Neuropathy with liability to Pressure Palsies (HNPP), Hereditary Neuralgic Amyotrophy (HNA), Familal Idiopathic Facial Palsy and Familial carpal tunnel syndrome. Table of Contents I-HNPP II-HNA Familal carpal tunnel syndrom IV Familal Facial Palsy ... Bibliography I-HNPP First palsy episodes occur mainly before thirty years of age. Onset is usually acute with minor or absent compression.

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