Hereditary Spastic Paraplegia Hereditary spastic paraplegia (HSP), also called familial spastic paralysis,refers to a group of genetic disorders. http://neurology.health-cares.net/hereditary-spastic-paraplegia.php
Extractions: showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping List of neurological disorders Wikipedia List of neurological disorders This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome Contents: Top A B C ... Z Canavan disease Carpal tunnel syndrome (CTS) Causalgia Central pain syndrome Central pontine myelinolysis Cephalic disorder Cerebral aneurysm Cerebral arteriosclerosis Cerebral atrophy Cerebral gigantism Cerebral palsy Charcot-Marie-Tooth disease Chiari malformation Chorea Chronic inflammatory demyelinating polyneuropathy
Alpers' Disease: Definition And Much More From Answers.com progressive cerebral poliodystrophy n. A familial spastic paralysis of theextremities occurring in infants and young children in which seizures, http://www.answers.com/topic/alpers-disease
Extractions: n. A familial spastic paralysis of the extremities occurring in infants and young children in which seizures, blindness, and deafness develop during the first year of life, accompanied by progressive destruction and degeneration of neurons of the cerebral cortex. Also called Alpers' disease Christensen-Krabbe disease Wikipedia Alpers' disease Alpers' disease , also called progressive infantile poliodystrophy , is a progressive degenerative disease of the central nervous system that occurs in infants and children. It is an autosomal recessive disorder that is sometimes seen in siblings. First signs of the disease, which include intractable seizures and failure to meet meaningful developmental milestones, usually occur in infancy, after the first year of life, but sometimes as late as the fifth year. Primary symptoms of the disease are developmental delay, progressive mental retardation , hypotonia (low muscle tone), spasticity (stiffness of the limbs) possibly leading to quadriplegia , and progressive dementia . Seizures may include epilepsia partialis continua, a type of seizure that consists of repeated myoclonic (muscle) jerks.
Neurological Diseases And Disorders Hereditary Spastic Paraplegia (also called familial spastic paralysis).Hereditary Spastic Paraplegia Fact sheet with a description of these disease that http://home.earthlink.net/~electrikmonk/Neuro/inDis.htm
Neurological Disorders - Medical Encyclopedia Fabry s disease; Fahr s syndrome; Fainting; familial spastic paralysis;Febrile seizures; Fisher syndrome; Friedreich s ataxia http://www.nursingstudy.com/encyclopedia/list_of_neurological_disorders.html
Extractions: Surgical Procedures This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome). A B C D ... Z Canavan disease Carpal tunnel syndrome CTS Causalgia Central pain syndrome Central pontine myelinolysis Cephalic disorder Cerebral aneurysm Cerebral arteriosclerosis Cerebral atrophy
Encyclopedia: List Of Neurological Disorders Fabry s disease Fahr s syndrome Fainting; familial spastic paralysis Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis http://www.nationmaster.com/encyclopedia/List-of-neurological-disorders
Extractions: Related Articles People who viewed "List of neurological disorders" also viewed: List of diseases starting with B List of rare diseases starting with A Williams syndrome Shy_Drager syndrome ... Canavan disease What's new? Our next offering Latest newsletter Student area Lesson plans Recent Updates Rafael Nadal Rachel Maddow RPG Maker Quinoa ... More Recent Articles Top Graphs Richest Most Murderous Most Taxed Most Populous ... More Stats Updated 54 days 15 hours 33 minutes ago. Other descriptions of List of neurological disorders This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome Neurology is a branch of medicine dealing with disorders of the central and peripheral nervous systems. ... Back pain is pain felt in the back that may come from the spine, muscles, nerves, or other structures in the back. ... Aphasia is a loss or impairment of the ability to produce or comprehend language, due to brain damage. ...
List Of Neurological Disorders -- Facts, Info, And Encyclopedia Article familial spastic paralysis (Click link for more info and facts about Febrileseizures) Febrile seizures Fisher syndrome (Click link for more info and facts http://www.absoluteastronomy.com/encyclopedia/L/Li/List_of_neurological_disorder
Extractions: This is a list of major and frequently observed (A disorder of the nervous system) neurological disorder s (e.g. (Click link for more info and facts about Alzheimer's disease) Alzheimer's disease ), symptoms (e.g. (Click link for more info and facts about back pain) back pain ), signs (e.g. (Inability to use or understand language (spoken or written) because of a brain lesion) aphasia ) and syndromes (e.g. (Click link for more info and facts about Aicardi syndrome) Aicardi syndrome Acquired Epileptiform Aphasia
Extractions: Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders-you are in this section Funding ... Jobs and Training You are here: Home Disorders The nation's leading supporter of biomedical research on disorders of the brain and nervous system. More about a disorder Clinical Trials Research Literature Press Releases NINDS Search (search help) Contact Us My Privacy NINDS is part of the National Institutes of Health Browse All Disorders (includes synonyms and research topics) Request mailed brochures Disorders beginning with the letters: A to F G to L M to S T to Z A To F - Select first letter of topic: A B C D ... F G To L - Select first letter of topic: G H I J ... L M To S - Select first letter of topic: M N O P ... S T To Z - Select first letter of topic: T U V W ... Z Absence of the Septum Pellucidum
Introduction: Hereditary Spastic Paraplegia - CureResearch.com Hereditary Spastic Paraplegia Hereditary spastic paraplegia (HSP), also calledfamilial spastic paralysis, refers to a group of genetic disorders that are http://www.cureresearch.com/h/hereditary_spastic_paraplegia/intro.htm
Extractions: Hereditary Spastic Paraplegia: 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. Researching symptoms of Hereditary Spastic Paraplegia: Further information about the symptoms of Hereditary Spastic Paraplegia is available including a list of symptoms of Hereditary Spastic Paraplegia , other diseases that might have similar symptoms in differential diagnosis of Hereditary Spastic Paraplegia , or alternatively return to research other symptoms in the symptom center Misdiagnosis and Hereditary Spastic Paraplegia: Research more detailed information about misdiagnosis of Hereditary Spastic Paraplegia , or research misdiagnosis of other diseases Treatments for Hereditary Spastic Paraplegia:
Extractions: Verified by National Institutes of Health Clinical Center (CC) May 16, 2005 Sponsored by: National Institute of Neurological Disorders and Stroke (NINDS) Information provided by: National Institutes of Health Clinical Center (CC) ClinicalTrials.gov Identifier: Purpose The purpose the study is to determine the genetic causes of specific voice disorders that run in families. Researchers are particularly interested in two conditions; 1. Spasmodic dysphonia 2. Vocal fold paralysis Familial vocal fold paralysis can be a life-threatening disorder that can cause difficulty with vocal fold movement for breathing and voice and sometimes for swallowing. Studies are ongoing at the NIH to better understand the pathophysiology and to relate it to the genetic pattern of inheritance. Families are being recruited to participate in these studies and are being provided with further information on the disorder and genetic counseling if desired. Physician referral is requested for affected members of families with vocal fold paralysis of an unknown cause occurring over at least 2 generations. All travel, lodging, examination and counseling costs are covered for both affected and unaffected members of a family. Examinations include: voice, laryngeal, neurological, electrodiagnostic testing, genetic counseling, and radiological studies. Condition
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Facial spastic paraplegia, familial spastic paraplegia, familial spastic paraparesis, French settlement dsease, hereditary spastic paraparesis, hereditary spastic paraplegia, paraplégie spasmodique familiale (French), spasmodic infantile paraplegia, spastic congenital paraplegia, spastic familial paraplegia, spastic familial paralysis, spastic infantile paralysis, spastic spinal familial paralysis A familial form of paraplegia characterized by spasticity hypertonicity and weakness - limited mainly to the lower extremities. This is followed by involvement of upper limbs, dysarthria, and dysphagia. Degeneration of the pyramidal tract of the spinal cord and of the columns of Goll is the principal histological feature. Ocular complications may include strabismus, pupillary defects, macular degeneration, and optic atrophy. Occurs in either sex, but is more common in young males. This is a very rare disease, with a frequency of about 1 in 30.000 persons. It is most common in Nordic countries. Inheritance is autosomal recessive (usually), or sex-linked.
Www.whonamedit.com A familial form of intermittent hypocalcaemic paralysis. spastic paraplegiaof the lower extremities and mental retardation in children with congenital http://www.whonamedit.com/syndlist.cfm/103
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Albert Mouchet's syndrome (Mouchet's paralysis) A historical term for a paralysis of the cubital nerve following fractures of the external condyle of the humerus in childhood. Albright-Hadorn syndrome A now obsolete eponym used to indicate the occurrence of paroxysmal hypokalemic muscular paralysis associated with osteomalacia in patients with renal tubular acidosis. Balint's syndrome A syndrome combining paralysis of visual fixation, optic ataxia, and impairment of visual fixation. Balint-Holmes syndrome (Balint's syndrome) A syndrome combining paralysis of visual fixation, optic ataxia, and impairment of visual fixation.
SPF - Spastic Paraplegia Foundation Home Page HSP is also known as Hereditary spastic Paraparesis, familial spastic Strümpell Disease, Hereditary CharcotDisease, spastic Spinal paralysis, http://sp-foundation.org/
Extractions: E-News Bulletins: Aug.-Sept. June-July April-May Meet John K. Fink, MD, SPF Medical Advisor and Teepu Siddique, MD, top researchers of HSP and PLS. Also: programs on assistive technology and adaptive equipment and more. Details here The SPF is the only non-profit organization in the Americas dedicated to neurodegenerative disorders called Primary Lateral Sclerosis (PLS) and Hereditary Spastic Paraplegia* (HSP). These diseases slowly attack one's ability to walk, causing levels of disability ranging from needing a cane to a wheelchair. In PLS, they generally also rob people of their ability to use their hands and arms, and even to speak. In very rare forms of HSP, they can cause mental retardation, dementia, epilepsy or other neurological problems. The Spastic Paraplegia Foundation is a 100% volunteer-managed and operated organization devoted to finding the causes and cures for these diseases and to providing critical information and support programs to people affected by them. We are enormously grateful to our
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 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: Submit a response ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Murillo, F. M. Articles by Hoffman, E. P. Neurology Articles H. Kobayashi, MD, PhD E. Pegoraro, MD, PhD G. Galluzzi, PhD G. Creel, MD C. Mariani, MD E. Farina, MD E. Ricci, MD G. Alfonso, MD R. M. Pauli, MD, PhD and E. P. Hoffman, PhD OBJECTIVE: To characterize a new gene locus for familial spastic paraparesis (FSP). BACKGROUND: FSP is a genetically heterogeneous group of upper motor neuron syndromes. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked disorder. Four loci for autosomal dominant FSP have been genetically mapped, and
