Extractions: Medical Encyclopedia Encyclopedia Disease G -> Guillain-Barre Guillain-Barre Alternate Names: Landry-Guillain-Barre syndrome; Acute idiopathic polyneuritis; Infectious polyneuritis; Acute inflammatory polyneuropathy Causes and Risks: Guillain-Barre syndrome is an acute type of nerve inflammation. The inflammation damages portions of the nerve cell, resulting in muscle weakness or paralysis . The damage usually includes loss of the myelin sheath of the nerve demyelination ) ,which slows conduction of impulses through the nerve. The damage may also include destruction of the axon part of the nerve cell (denervation), which blocks conduction through the nerve. The exact cause of this disorder is not known. It usually follows a minor infection, usually a respiratory (lung) infection or gastrointestinal (gut) infection. The signs of the infection usually have disappeared before the signs of Guillain-Barre begin. It may occur at any age but is most common in people of both sexes between the ages 30 and 50.
Extractions: The text presented on these pages is for your information only. It is not a substitute for professional medical advice. It may not represent your true individual medical situation. Do not use this information to diagnose or treat a health problem or disease without consulting a qualified health care provider. Please consult your health care provider if you have any questions or concerns.
Extractions: (advertisement) Synonyms, Key Words, and Related Terms: GBS, acute idiopathic polyneuritis Background: Classic Guillain-Barré syndrome (GBS) is an acute, ascending, and progressive neuropathy characterized by weakness, paresthesias, and hyporeflexia. In severe cases, muscle weakness may lead to respiratory failure. Severe labile autonomic dysfunction also may occur. Maximal weakness typically occurs 2 weeks after the initial onset of symptoms but may evolve early and abruptly. In the early 1900s, Guillain, Barré, and Strohl first described the syndrome in 2 patients who spontaneously recovered from a progressive ascending motor weakness with areflexia, paresthesias, sensory loss, and an elevated level of cerebrospinal fluid (CSF) protein. Since the polio vaccine came into widespread use, GBS has become the most common remaining cause of acute neuromuscular paralysis. Pathophysiology: Most patients with GBS exhibit absent or profoundly delayed conduction in action nerve fibers. This aberrant conduction results from demyelination of nerve cell axons. Peripheral nerves and spinal roots are the major sites of demyelination, but cranial nerves also may be involved. GBS is believed to result from an autoimmune response triggered by an antecedent illness or by any of a long list of medical conditions. The autoimmune response seems to have both humoral and cell-mediated components. In most patients with GBS, symptoms result from injury to the myelin sheath. In a subset of patients with GBS, axonal damage results from a direct cellular immune attack on the axon itself.
Med Help General Library Glaucoma Primary Open Angle Glaucoma Gonorrhea Gout Granuloma Inguinale (donovanosis)GuillainBarre Syndrome (acute idiopathic polyneuritis) Guillain-Barre http://users.westnet.gr/~aesclep/general.htm
EnableNet - Enablenet.browse.browse illness. Book Guillain Barre Syndrome (acute idiopathic polyneuritis) An overview for the layperson. Book No surrender. Book Guillain http://www.enable.net.au/index.cfm?fuseaction=enablenet.browse.browse&catid=2234
CANADIAN GuillainBarre Syndrome, also known as Landry's Ascending Paralysis, Acute IdiopathicPolyradiculneuritis and acute idiopathic polyneuritis, is an inflammatory http://www.canadianneuropathyassociation.org/Newsletter01Vol01.htm
Extractions: CANADIAN EUROPATHY ASSOCIATION Summer 2002 Vol. 1 This is the Canadian Neuropathy Associations first newsletter. The Canadian Neuropathy Association is a Not-For-Profit organization whose mandate is 'Education, Research, and Support. We have been active for approximately two years now and are in the process of becoming a charity as well. It is our hope that our newsletters will be informative and thought provoking. However, we cannot stress strongly enough that the information provided in the newsletter should never replace seeking competent medical advice. The Editors, our Board and our contributors do not claim to have any medical training or other competencies that could be construed as offering treatments or cures. The goal of our newsletters is to inform readers and to encourage readers to advocate for themselves. It is also our hope that they will share any knowledge they may have with us for future newsletters. One more note: At an American Medical Association AMA panel discussion in New York in July 1997 it was stated that some of pain cases are misdiagnosed
ThirdAge - Adam - Guillain-Barre Syndrome Alternative Names LandryGuillain-Barre syndrome; acute idiopathic polyneuritis;Infectious polyneuritis; Acute inflammatory polyneuropathy. Symptoms http://www.thirdage.com/health/adam/ency/article/000684sym.htm
Extractions: document.write(''); document.write(''); document.write(''); document.write(''); document.write(''); document.write(''); document.write(''); document.write(''); Activities Computers Family Tree Health ... Prevention Alternative Names: Landry-Guillain-Barre syndrome; Acute idiopathic polyneuritis; Infectious polyneuritis; Acute inflammatory polyneuropathy Symptoms: The disorder progresses rapidly (from days to a few weeks), causing w eakness or paralysis in a symmetrical manner. As weakness starts in the legs and then spreads to the arms, it is referred to as ascending paralysis. At the same time, patients may notice tingling, foot or hand pain, and clumsiness. As paralysis worsens, the patient may require assisted ventilation in order to breathe. The phases of the illness include an initial phase of rapid worsening that may take only a few hours to reach the most severe symptoms. This phase can last up to 3 weeks. This is followed by a plateau phase of no changes, then a recovery phase where symptoms improve over days to 6 months or longer. Typical symptoms include the following: Muscle weakness or paralysis (the most common symptom) or uncoordinated movements Weakness begins in the feet and legs and may progress upward to the arms and cranial (head) nerves May progress rapidly over 24 to 72 hours May begin in the arms and progress downward May occur in the arms and legs at the same time
UK Self Help Groups: A Acute Anxiety Disorder. see under Phobia. acute idiopathic polyneuritis. contactGBS Support Group, Tel 01529 304 615/Helpline 0800 374 803. AdamsOliver Syndrome. http://www.ukselfhelp.info/a.htm
Extractions: Main Index IMPORTANT - Please use www.ukindex.info and/or the links at the foot of this page to help maintain this free resource. Adoption UK , Tel 01295 660 121/Helpline 0870 7700 450 BAAF Adoption and Fostering , Tel 020 7593 2000 Fostering Network , Tel 020 7620 6400 Natural Parents Network , Tel 01273 307 597 NCH Action for Children , Tel 020 7704 7000 NORCAP , Tel 01865 875 686 Post Adoption Centre , Tel 020 7284 0555
VII: Disorders Of Myelin And Peripheral Nerve acute idiopathic polyneuritis (LANDRYGUILLAIN-BARRÉ SYNDROME). Approximatelyhalf of the cases are associated with an antecedent viral infection. http://www.borg.labmed.umn.edu/PathClass/5102/neuro/clark7.html
Extractions: Back Home VII. DISORDERS OF MYELIN AND PERIPHERAL NERVE A. MYELIN, GENERAL PRINCIPLES PNS MYELIN CNS MYELIN Schwann cell origin Oligodendroglial origin One internode per Schwann cell Multiple internodes per oligodendrocyte EM: prominent collar of Schwann cell EM: inconspicuous cytoplasmic collar cytoplasm with basal lamina with no basal lamina Nodes of Ranvier with complex interdigitated Nodes of Ranvier have no covering by Schwann cell processes and basal lamina cell processes or basal lamina PNS and CNS myelin differ somewhat in their composition of proteins and lipids B. DISEASES OF MYELIN Two groups of disorders affect myelin selectively and leave neurons (axons) wholly or relatively intact:. Aquired disorders of myelin are called demyelinating diseases and genetic (metabolic) disorders of myelin are called dysmyelinating diseases or leukodystrophies . Disorders of CNS myelin primarily affect white matter but may also affect gray matter regions containing numerous myelinated axons. C DEMYELINATING DISEASES MULTIPLE SCLEROSIS a) General - The prototype of demyelinating diseases - Worldwide distribution - highest prevalence in temperate zones - Higher prevalence in Northern than Southern states - high in Minnesota - Common in young people (20-40 years), mean age of onset ~ 30.
Glossary L back.gif (1031 bytes). lachrymation lachrimation. Secretion of tears, especiallyin excess. landry's paralysis Landry's syndrome, acute idiopathic polyneuritis. http://www.nutritionfocus.com/nutrition_supplementation/glossary/GlossaryL.html
Searchalot Directory For A Protein C Resistance (5); acute idiopathic polyneuritis (14); Addictionand Recovery (26); Addison's Disease (17); Adie Syndrome (5); Adiposis http://www.searchalot.com/Top/Health/ConditionsandDiseases/A/
Extractions: Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases : A All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo!
WebGuest - Open Directory Health Conditions And Diseases A Neuroma@ (15); Acrodynia@ (3); Acromegaly@ (5); Activated ProteinC Resistance@ (5); acute idiopathic polyneuritis@ (14); ADD and ADHD http://directory.webguest.com/index.cgi/Health/Conditions_and_Diseases/A/
Mandy Siu Yu Lung 2246419 ray) Syndrome, named in honour of the French neurologists who described the conditionin two soldiers in 1916, is also called acute idiopathic polyneuritis. http://www.micro.unsw.edu.au/MICR3051 2001/Pudadera, Mai, Wood Lung/mandy.html
Extractions: Guillain-Barre (Ghee-yan Bah-ray) Syndrome, named in honour of the French neurologists who described the condition in two soldiers in 1916, is also called acute idiopathic polyneuritis. It is believed to be an autoimmune disease, in which macrophages and T-cells attack the myelin sheath covering of nerve cells and nerve axons (the extension of the nerve cell that conducts impulses away from the nerve cell body) in peripheral and cranial nerves, resulting in a block or delay in nerve signal transmission. Complications in the central nervous system are very rare. It usually affects the motor nervous system which makes the muscles work, leading to loss of sensation or muscle weakness in the corresponding muscles that are innervated by the affected nerves. In more serious cases the absent of reflexes, complete paralysis and breathing difficulty due to the weakening of respiratory muscles may also occur.
Directory :: Look.com Neurology Channel A description of GuillainBarre syndrome, also knownas Landry's ascending paralysis and acute idiopathic polyneuritis. http://www.look.com/searchroute/directorysearch.asp?p=526369