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Hereditary Spastic Paraplegia: more detail

The Official Patient's Sourcebook on Hereditary Spastic Paraplegia: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09

Hereditary spastic paraplegia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Chitra, MBBS, MD Venkatasubramanian, 2005

Hereditary spastic paraplegia: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Sandra Galeotti, 2005

On hereditary ataxia and spastic paraplegia (The treasury of human inheritance) by Julia Bell, 1939

lists with details

The First International Symposium For Hereditary Spastic Paraplegia
NINDS is part of the National Institutes of Health Contact us . Content for thispage. The First International Symposium for hereditary spastic paraplegia.
http://accessible.ninds.nih.gov/news_and_events/spastic_paraplegia.htm

Extractions: News and Events - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders ... Find People The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury Current Archived Events Proceedings ... NINDS Notes Current Archived Upcoming Archived Labs at NINDS NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us Get Web page suited for printing
Nature Publishing Group
4 pp 347 348 SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegiaHeema Patel, Harold Cross, Christos Proukakis, Ruth Hershberger, Peer Bork
http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v31/n4/full/ng937.ht
SPF - Home Page
Other names used for HSP are hereditary spastic paraplegia, Familial Spastic Paraparesis(or paraplegia), Spastic Paraplegia, Strümpell Disease, Strümpell
http://www.sp-foundation.org/

Extractions: NEW: Cookbook! Info Here 2003 Research Grant Program The SPF is a non-profit organization dedicated to neurological disorders Hereditary Spastic Paraparesis* (HSP) and Primary Lateral Sclerosis (PLS). Information on the SPF here and on the disorders here SPF VISION: The day where all individuals with HSP or PLS are diagnosed, treated and cured. SPF MISSION: We are committed to: *Creating opportunities for mutual support and sharing Get information about HSP and PLS and about the SPF Information about the Disorders (PDF Format) Basic information English En español En français What's Happening in My Body? English En español To make a tax-deductable donation: Click here. To get involved, please use the email link below. Subscribe To The SPF E-News!
The FSP Page - Familial Spastic Paraparesis
Information about the spinal cord disorder known as Familial Spastic Paraparesis(FSP), also known as hereditary spastic paraplegia (HSP) or StrumpellLorrain.
http://www.geocities.com/HotSprings/Spa/2847/

Extractions: Hereditary Spastic Paraplegia Hereditary spastic paraplegia is an inherited spinal cord disorder characterized by gradual development of muscle weakness, spasms, and stiffness of the legs. Symptoms may be first noticed in early childhood, or at any age though adulthood. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms may appear, or the weakness and stiffness may spread to other parts of the body. The terms "Hereditary Spastic Paraplegia" (HSP) and "Familial Spastic Paraparesis" (FSP) are the commonly used names in the United States for this disorder. For those in Europe, "Strumpell-Lorrain" is probably more common. These terms all refer to the same set of disorders. Other names associated with this disease are Strümpell-Lorrain familial spasmodic paraplegia, Strümpell's familial paraplegia, spasmodic infantile paraplegia, spastic congenital paraplegia, spastic spinal familial paralysis, hereditary spastic paraparesis, and familial spastic paraplegia.
First International Symposium On Hereditary Spastic Paraplegia
National Institute of Neurological Disorders and Stroke (NINDS) and the Office ofRare Diseases First International Symposium On hereditary spastic paraplegia.
http://rarediseases.info.nih.gov/news-reports/workshops/herspaspara12000.html
Familial Spastic Paraplegia - For Patients And Families - The Center For Human G
For Patients and Families Familial Spastic Paraplegia/hereditary spastic paraplegia
http://www.chg.duke.edu/patients/fsp.html

Extractions: Familial spastic paraparesis/paraplegia (FSP) and hereditary spastic paraparesis/paraplegia (HSP) are names applied to a group of degenerative neurological disorders characterized by specific walking problems. Physicians are now applying the diagnosis of hereditary spastic paraparesis/ paraplegia to patients whose leg muscles have symptoms of spasticity (stiffness and/or spasms), paraparesis (weakness), or paraplegia (paralysis), especially when similar symptoms occur in other members of the patients family due to inherited DNA changes (hereditary symptoms). Currently physicians use the familial spastic paraparesis/ paraplegia diagnosis for cases with similar symptoms that may result from family members exposure to shared environmental factors, rather than to genetic causes. FSP/HSP may vary from family to family and patient to patient.
Health Library - Paraplegia, Hereditary Spastic
hereditary spastic paraplegia (HSP) is a group of inherited neurological disorderscharacterized by progressive weakness (paraplegia) and increased muscle tone
http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=
Hereditary Spastic Paraplegia
The Official Patient's Sourcebook on hereditary spastic paraplegia (Familial SpasticParaplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell
http://www.icongrouponline.com/health/Hereditary_Spastic_Paraplegia.html

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 Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) 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
Hereditary Spastic Paraplegia. Hereditary Spastic Paraplegia
hereditary spastic paraplegia. hereditary spastic paraplegia The thelegs. What is hereditary spastic paraplegia? Information about
http://www.cerebralpalsy.de/hereditary-spastic-paraplegia.asp
Spastic. Spastic
n) a collection of thoughts, images, profundities and pretentions assembled inhypertext markup language hereditary spastic paraplegia Hereditary spastic
http://www.cerebralpalsy.de/spastic.asp
Hereditary Spastic Paraplegia : Meddie Health Search
ITEMS LINKS GeneClinics An Overview In depth details about hereditaryspastic paraplegia. Includes a summary, definition, categories
http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/He
Hereditary Spastic Paraplegia
Print this article. Find related articles By topic Neurology. By keywordsReceive HealthLink via email! Subscribe now . hereditary spastic paraplegia.
http://oci.mcw.edu/article/921730935.html

Extractions: Subscribe now >> Hereditary spastic paraplegia (HSP), also called familial spastic paralysis, refers to a group of genetic disorders that are characterized by progressive weakness and spasticity (stiffness) of the legs. Symptoms of HSP may occur alone or, in more complicated forms of HSP, may occur in combination with a number of other neurological symptoms. Generally, the primary feature is severe, progressive, lower extremity spasticity. The spasticity sometimes occurs with abnormalities such as optic neuropathy, retinopathy (disease of the retina), dementia, ataxia (lack of muscle control), ichthyosis (a skin disorder causing dry, rough, scaly skin), mental retardation, and deafness. There is no specific treatment to prevent, slow, or reverse HSP's progressive disability. Treatment is symptomatic. The prognosis for individuals with HSP varies greatly. Some cases are seriously disabling while others are less disabling and are compatible with a productive and full life. The majority of individuals with HSP have a normal life expectancy.
Arch Neurol -- Page Not Found
hereditary spastic paraplegia and Hereditary Ataxia Part 2 A Family DemonstratingVarious Phenotypic Manifestations With the SCA3 Genotype Author Information
http://archneur.ama-assn.org/issues/v57n5/abs/noc90036.html

Extractions: The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"
Arch Neurol -- Page Not Found
Spectrum of SPG4 Mutations in a Large Collection of North American Families Withhereditary spastic paraplegia Author Information Inge A. Meijer, BSc; Collette
http://archneur.ama-assn.org/issues/v59n2/abs/noc10231.html

Extractions: The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"
ClinicalTrials.gov - Linking Patients To Medical Research: Results
Search results for hereditary spastic paraplegia ALLFIELDS are shown below.Show all trials, including those no longer recruiting patients.
http://www.clinicaltrials.gov/search/term=Hereditary Spastic Paraplegia
ClinicalTrials.gov - Linking Patients To Medical Research: Study Details
Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis,hereditary spastic paraplegia and Amyotrophic Lateral Sclerosis.
http://www.clinicaltrials.gov/ct/gui/show/NCT00023075?order=1
Medical Dictionary Online : X-linked Recessive Hereditary Spastic Paraplegia
Xlinked Recessive hereditary spastic paraplegia on the Free Online MedicalDictionary. X-linked Recessive hereditary spastic paraplegia.
http://www.online-medical-dictionary.org/medical-dictionary-x/X-linked-Recessive
Genetics Of Hereditary Spastic Paraplegia
Genetics of hereditary spastic paraplegia. Wednesday, September 04, 2002.hereditary spastic paraplegia with identified gene loci or mutations
http://www.angelfire.com/retro/michaelpoon168/genetics_of_hereditary_spastic_par

Extractions: Michael Poon's Shrine of Neurology HOME CONTENTS CONTACT US HOME ... CONTACT US Genetics of hereditary spastic paraplegia Wednesday, September 04, 2002 Hereditary spastic paraplegia with identified gene loci or mutations Notation Inheritance Gene location Gene identified XR XR Proteolipid protein AD AD Spastin AR AD AR Paraplegin AD AD AD AR AD AD AR AD = autosomal dominant; AR = autosomal recessive; XR = X-linked recessive.
The Association Of Hereditary Spastic Paraplegia And Hereditary Motor And Sensor
The association of hereditary spastic paraplegia and hereditary motor andsensory neuropathy in the same family Münife Müftüoðlu 1 , MD, Ý.
http://medicine.inonu.edu.tr/dergi/Contents/Volume2/Issue2/Abstract/193-195.html

Extractions: The association of hereditary spastic paraplegia and hereditary motor and sensory neuropathy in the same family Münife Müftüoðlu , M.D., Ý. Özcan Ertürk , M.D., Cemal Özcan , M.D., Hakan Ekmekçi , M.D. The association of hereditary spastic paraplegia (HSP) and sensory neuropathies have been reported in a number of cases. But it is rare to detect both entities seperately in different members of the same family. In the present study, we report clinical and electrophysiological findings of three members of a family. In two of the siblings the clinical picture was indistinguishable from "pure" hereditary spastic paraplegia, but electrophysiological studies revealed a predominantly sensory polyneuropathy. In the third case (the mother of the siblings), the clinical diagnosis was consistent with hereditary motor sensory neuropathy type 2, which was also confirmed by electrophysiological studies. We believe that, with the further genetic reevaluations, the hereditary spastic paraplegia with sensory abnormalities may take a new place in the classification of hereditary motor and sensory polyneuropathies, as a distinct entity.[Journal of Turgut Özal Medical Center 2(2):193-195,1995] Key Words : Hereditary spastic paraplegia, hereditary motor and sensory neuropathy
FSG/HGP - Recent CHG Publications - The Center For Human Genetics - Duke Univers
Familial Spastic Paraplegia/ hereditary spastic paraplegia. A kinesin heavychain (KIF5A) mutastion in hereditary spastic paraplegia (SPG10).
http://wwwchg.mc.duke.edu/research/fspx.html

Extractions: Editorial: Crosby AH and Proukakis C. Is the transporation highway the right road for hereditary spastic paraplegia? Am J Hum Genetics 71:000, 2002 Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany R-MN, Vance JM, Scott WK, and Pericak-Vance MA. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia. Neurogenetics 3(2):91-97, 2001 Svenson IK, Ashley-Koch AE, Gaskell PC, Riney TJ, Cumming WJ, Kingston HM, Hogan EL, Boustany RN, Vance JM, Nance MA, Pericak-Vance MA, Marchuk DA. Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia. Am J Hum Genet 68(5):1077-1085, 2001

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