Neurological Syndromes spastic weakness/paralysis in all four limbs or Degenerative Disorders,Bouvier des Flandres myopathy; familial dysphagia; central core myopathy; http://www.ivis.org/special_books/Braund/braund1/chapter_frm.asp?LA=1
ANNALS ONLINE -- Sign In Page familial presenile dementia with spastic paralysis. J. Neurol. Psychopathol.2734. Griffiths, R., T. Mortimer, D. Oppenheimer J. Spalding. 1982. http://www.annalsnyas.org/cgi/content/full/903/1/129
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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 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.
List Of Diseases: F - CureResearch.com familial rickets type of Xlinked Dominant Genetic Diseases; familial spasticParalysis see Hereditary spastic Paraplegia Fanconi s syndrome http://cureresearch.com/lists/condsf.htm
Extractions: Malpractice A B C D ... Z Fabry's Disease Fabry's Disease of female carrier ... type of Fabry's Disease Face bone fracture ... see Face fracture Face fracture Facial cellulitis ... type of Cellulitis Facial conditions ... type of Head Conditions Facial fracture Facioscapulohumeral Muscular Dystrophy ... type of Muscular Dystrophy Factitious diabetic pill ingestion ... type of Factitious syndromes Factitious disorder NOS ... type of Factitious syndromes Factitious insulin ... type of Factitious syndromes Factitious syndromes Fahr's Syndrome Failure To Thrive Fainting ... see Syncope Falciparum malaria ... type of Malaria Fall-related hip fracture ... type of Hip fracture Fallen bladder ...
Familiar Familial Prionlike Disorders The disease was first described in 1933 as familial presenile dementia withspastic paralysis. See. Plant, GTet al Brain 113, 721747 (1990) case http://www.mad-cow.org/med_fever.html
Extractions: Dentatorubralpallidoluysian atrophy: are fibrils congophilic? 10 June 99 webmaster (based on Medline, OMIM, etc.) Familial Mediterranean fever (FMF) is a autosomal recessive inflammatory disease frequently complicated by reactive systemic amyloidosis, recurring attacks of fever, synovitis, or serositis. The amyloid is formed of a common amyloid constituent, SAA (serum amyloid A) protein. However, after years of understandable confusion , the FMF susceptibility locus ( MEFV ) was mapped to chromosome 16p13 it encodes a 3.7-kb transcript expressed almost exclusively in mature granulocytes. The corresponding 781-amino acid protein, pyrin (or marenostrin), has no sequence similarity to the SAA amyloid .protein [see below]. Mutations clustered in exon 10 (M680V, M694I, M694V, I692del, K695R, A744S, and R761H and V726A), exon 2 (E148Q, E167D and T267I), exon 3(P369S), and exon 5 (F479L) account for most known familial cases.
Français / its international name is familial spastic Paraplegia or Hereditary spastic Hereditary spastic Paraplegia is the degeneration of the spinal cord http://assoc.wanadoo.fr/asl.spastic/anglasl/englindx.htm
Extractions: in progress Hereditary Spastic Paraplegia is the degeneration of the spinal cord which is visible through walking problems which slowly develop to paralysis of the legs. You will find a brief presentation in the brochure ( la brochure , a more detailed one in the technical sheet ( la fiche technique ) a page on the main symptoms ( ,) and another with a glossary ( glossaire of technical and scientific terms. Medical Information le conseil scientifique de l'A.SL la recherche The Association qu'est-ce que l'A.SL ? aspect social vivre avec trucs et astuces Publications and current projects brochure fiche technique revue trimestrielle film ... LAST CONGRESS brochure / technical sheet / quarterly newsletter / film / forum / special editions / medical and association projects The environment SCD EURO equivalent foreign sites SCD Euro interesting links Contacts Write to the Chairman Jean-Pierre Blois / write to the Webmaster Philippe Grammont Any comment about these pages will be welcome. The site is run by the founder member of A.SL, who suffers from the illness and uses only the experience he has gained. In no way can the contents of these pages be used for medical diagnosis. Please consult your doctor.
Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Neurology Neuromuscular Diseases Last Updated: August 25, 2005 Rate this Article Email to a Colleague Synonyms and related keywords: PLS, motor neuron disease, motoneuron disease, progressive spasticity, stiffness, MNDs AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Carmel Armon, MD, MSc, MHS , Professor of Neurology, Tufts University School of Medicine; Chief, Division of Neurology, Baystate Medical Center Carmel Armon, MD, MSc, MHS, is a member of the following medical societies: American Academy of Neurology American Academy of Sleep Medicine American Association of Neuromuscular and Electrodiagnostic Medicine American Clinical Neurophysiology Society ... Movement Disorders Society , and Sigma Xi Editor(s): Paul E Barkhaus, MD
The Health Library Nervous System And Brain InfantileOnset Ascending Hereditary spastic ParalysisGenetics Home Reference, NLM Fatal familial Insomnia. Fatal familial InsomniaMerck Manual http://healthlibrary.stanford.edu/resources/internet/bodysystems/neuro_degenerat
Extractions: Diseases and Disorders Use these links to jump directly to your topic of interest in Nervous System and Brain: Signs and Symptoms: Pain Neurologic Manifestations Language Disorders Perceptual Disorders Central Nervous System: Brain Diseases Brain Injury Infections Malformations ... Tumors Other Diseases and Disorders: Autoimmune Nervous System Diseases Autonomic Nervous System Diseases Cranial Nerve Disorders Degenerative Nervous System Diseases ... Sleep Disorders Other Topics: General Nervous System and Brain Anatomy Diagnostic Procedures Neural Transplantation Degenerative Nervous System Diseases (Jump to: Ataxia: General Information Episodic Ataxia Friedreich's Ataxia Spinocerebellar Ataxia ... Other Ataxias Prion Diseases: General Information Bovine Spongiform Encephalopathy Chronic Wasting Disease Creutzfeldt-Jakob Disease ... Kuru Other Degenerative Diseases: Dyssynergia Cerebellaris Progressiva Hereditary Spastic Paraplegia Huntington's Disease Neurodegeneration with Brain Iron Accumulation ... Wolfram Syndrome Ataxia General Information What is Ataxia?:National Ataxia Foundation Coordination Disorders:Merck Manual Pediatric Ataxia:We Move The Physician's Guide to Hereditary Ataxia:NORD ... Hereditary Ataxia Overview:GeneReviews Episodic Ataxia Episodic Ataxia:UCSF Episodic Ataxia Type 2:GeneReviews Friedreich's Ataxia Friedreich's Ataxia Fact Sheet:NINDS Friedreich's Ataxia FAQ:Friedreich's Ataxia Parents Group Friedreich's Ataxia:Muscular Dystrophy Association Friedreich Ataxia:Rehabinfo Network ... Friedreich Ataxia:GeneReviews Spinocerebellar Ataxia Ataxias and Cerebellar/Spinocerebellar Degeneration:NINDS Spinocerebellar Ataxia:Rehabinfo Network Machado-Joseph Disease Fact Sheet (Spinocerebellar Ataxia Type 3):NINDS Machado Joseph Disease:Jewish Genetic Diseases ... Spinocerebellar Ataxia: Making an Informed Choice About Genetic Testing:University of Washington [PDF]
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FIRSTConsult - Sdfdsf familial spastic paraparesis (Hereditary spastic paraplegia) Causes presynapticparalysis of myoneural junctions and reduces abnormal contractions http://www.firstconsult.com/?action=view_article&id=1014454&type=101&bref=1
Login Hereditary spastic paraplegia (HSP) is a clinically and genetically Maia M (1974)Strumpell s familial spastic paraplegia genetics and neuropathology. http://dx.doi.org/10.1086/302258
Dr. Fontaine CV Translate this page Hyperkalemic Periodic paralysis and the adult muscle sodium channel The phenotypeof pure autosomal dominant spastic paraplegia, Neurology, 44, http://www.periodicparalysis.org/PPA/POPUP.asp?POPUP_ID=37
THE MERCK MANUAL, Sec. 13, Ch. 162, Viral Diseases Tropical spastic Paraparesis/HTLVI-associated Myelopathy There is someevidence of a familial form from a case study in Brazil. http://www.merck.com/mrkshared/mmanual/section13/chapter162/162d.jsp
