Hereditary Spastic Paraplegia - General Practice Notebook hereditary spastic paraplegia. This is a hereditary neurodegenerative disorderwhich in its simple form results in a progressive spastic paraplegia. http://www.gpnotebook.co.uk/cache/825557023.htm
Extractions: Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous group of inherited disorders characterized by insidiously progressive, often severe, lower extremity weakness and spasticity. Symptom severity, age of onset and rate of disease progression may vary widely among patients. It is estimated that three in every 100,000 people are affected with HSP in the U.S. HSPs are classified by clinical presentation, as either uncomplicated or complicated, and by inheritance pattern. Uncomplicated (or pure) HSP is the most common form and is characterized by progressive lower extremity spastic weakness, accompanied by hypertonic urinary bladder disturbances, and often, mildly impaired vibration sensation. Uncomplicated HSP can be disabling, but it does not shorten life span. HSP is classified as complicated if the impairments of the uncomplicated form are accompanied by additional neurologic abnormalities that are not attributable to other co-existing disorders. Researchers estimate that uncomplicated HSP represents 90% of all HSP cases, while complicated HSP accounts for 10%.
Extractions: Fink, J. Hereditary spastic paraplegia. In: , 4th Edition, eds. David L. Rimoin et al., 3124-45. 2001. London:Churchill Livingstone. Muglia, M. et al., A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. J Neurol Stapley, C. Spastic Paraplegia or Hereditary Spastic Paraparesis General Information. In: HSPinfo.org http://hspinfo.org/HSP.htm Fink, J.K. Hereditary spastic paraplegia. Neurol Clin N Am Tessa, A. et al., SPG3A, An additional family carrying a new atlastin mutation. Neurology Zhao, X. et al., Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nat Genet Fink, J. Hereditary Spastic Paraplegia: The Pace Quickens. Ann Neurol Patel, H. SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia. Nat Genet Hazan, J. et al., Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet Fink, J. Hereditary spastic paraplegia: Clinical features. In: Hereditary Spastic Paraplegia (HSP) Research http://www.med.umich.edu/hsp/clinfeatures.htm
Diagnosing Hereditary Spastic Paraplegia Subject Diagnosing hereditary spastic paraplegia Topic Area Neurology GeneralForum The Neurology and Neurosurgery Forum Question Posted By Cheryl on http://www.medhelp.org/forums/neuro/archive/1298.html
Diagnosing Hereditary Spastic Paraplegia Subject Diagnosing hereditary spastic paraplegia Forum The Neurology and NeurosurgeryForum Topic Area Posted by Cheryl on July 28, 1997 at 130346 http://www.medhelp.org/forums/neuro/archive/1188.html
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:: Ez2Find :: Hereditary Spastic Paraplegia Guide hereditary spastic paraplegia, Global Metasearch Any Language Guides,hereditary spastic paraplegia. ez2Find Home Directory Health http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Hereditary Spastic Paraplegia Web Sites The FSP Support Group [Site Info] [Translate] [Open New Window] GeneClinics: An Overview [Site Info] [Translate] [Open New Window] In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources. URL: http://www.geneclinics.org/profiles/hsp/
Hereditary Spastic Paraplegia The New Health Directory, Directory, Home Health Conditions and DiseasesGenetic Disorders hereditary spastic paraplegia (6). HSPinfo http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/He
The FSP (Familial Spastic Paraplegia) Group Familial Spastic Paraplegia (FSP) is also known as hereditary spastic paraplegia(HSP), Familial Spastic Paraparesis or StrumpellLorrain Syndrome. http://www.fspgroup.org/
Extractions: Moving Forward Together Familial Spastic Paraplegia (FSP) is also known as Hereditary Spastic Paraplegia (HSP), Familial Spastic Paraparesis or Strumpell-Lorrain Syndrome. The condition is rare and is caused by the inheritance of an abnormal gene from an affected parent. It has been diagnosed where no family history of the condition is known. FSP describes a group of disorders characterised by progressive stiffness (spasticity) of the legs associated with varying degrees of weakness. A number of symptoms are associated with this condition including stiffness and leg cramps which often precede the emergence of a scissoring spastic gait. A quarterly newsletter which updates members on current topics. A national meeting which includes an Annual General Meeting, lectures by FSP specialists and subsequent discussion groups. A help-line which offers advice to new members and those with problems. A library of information articles on FSP.
Extractions: (Familial Spastic Paraplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell-Lorrain Familial Spasmodic Paraplegia; Strumpell-Lorraine Syndrome; Strumpell's Familial Paraplegia) 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 Hereditary Spastic Paraplegia. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Familial Spastic Paraplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell-Lorrain Familial Spasmodic Paraplegia; Strumpell-Lorraine Syndrome; Strumpell's Familial Paraplegia Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Hereditary Spastic Paraplegia: Guidelines
Extractions: Front Page Today's Digest Week in Review Email Updates ... Genetic Disorders Hereditary Spastic Paraplegia (6 links) News about Hereditary Spastic Paraplegia Scientists Confirm New Breast Cancer Gene (May 17, 2004) full story Researchers Confirm Genetic Link Between Hereditary Breast And Prostate Cancer (May 4, 2004) full story Researchers Discover New Clinical Syndrome Leading To Severe Osteoarthritis (May 4, 2004) full story Study Of Growth Hormone Treatment And Creutzfeldt-Jakob Disease Underscores Need For Prevention Of Adrenal Crises (April 7, 2004) full story Genetic Basis Of Hereditary Nerve Disorder Revealed (April 6, 2004)
Hereditary Spastic Paraplegia hereditary spastic paraplegia. hereditary spastic paraplegia (HSP),also called familial spastic paraparesis (FSP), refers to a group http://www.sciencedaily.com/encyclopedia/hereditary_spastic_paraplegia
Extractions: Front Page Today's Digest Week in Review Email Updates ... Outdoor Living Main Page See live article Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis (FSP), refers to a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs. Though the primary feature of HSP is severe, progressive, lower extremity spasticity , in more complicated forms it can be accompanied by other neurological symptoms. These include optic neuropathy, retinopathy (diseases of the retina), dementia ataxia (lack of muscle control), icthyosis (a skin disorder resulting in dry, rough, scaly skin), [[mental retardation]
NORD - National Organization For Rare Disorders, Inc. General Discussion hereditary spastic paraplegia (HSP) is a group of inherited neurologicaldisorders characterized by progressive weakness (paraplegia) and http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Paraplegia, H
Extractions: The FSP Support Group - For people suffering from Familial Spastic Paraplegia. Includes a newsletter, discussion forum, links, and contact details. GeneClinics: An Overview - In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources. Hereditary Spastic Paraplegia - HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke. Hereditary Spastic Paraplegia - In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs. MCW Healthlink: HSP - An article about hereditary spastic paraplegia, also called familial spastic paralysis. Spastic Paraplegia Foundation - Supports on the upper motor neuron disorders hereditary spastic paraplegia and primary lateral sclerosis. Information about these conditions, disability resources, newsletters, news, announcements, research and support.
SPG20 Is Mutated In Troyer Syndrome, An Hereditary Spastic ng937 volume 31 no. 4 pp 347 348 SPG20 is mutated in Troyer syndrome,an hereditary spastic paraplegia Heema Patel, Harold Cross http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v31/n4/full/ng937.ht
SPG20 Is Mutated In Troyer Syndrome, An Hereditary Spastic Published online 22 July 2002, doi10.1038/ng937 volume 31 no. 4 pp 347 348SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v31/n4/abs/ng937.htm