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categoría genética o congénita, músculos, neurología frecuencia poco común (U.S.) Usually seen in those 30 years or older.

riesgo por la edad

riesgo por la duración de los síntomas

otros tipos médico family practitioner internist neurologist neurosurgeon adolescent medicine código postal Buscar local Los resultados generados por computadora son sugerencias para ayudarle a encontrar un médico. MEDgle no recomienda ningún tipo de médico o pretenden ser completos o precisos en los proveedores y sugirió especialidades.

atrofia muscular espinal tipo 4 - enfermedad hereditaria que causa debilidad muscular del músculo Definición de atrofia muscular espinal tipo 4 Adult SMA - Type 4. Weakness usually begins in late adolesceence in tongue, hands, or feet then progresses to other areas of the body. más Adult SMA - Type 4. Weakness usually begins in late adolesceence in tongue, hands, or feet then progresses to other areas of the body. Course of disease is much slower and has little or no impact on life expectancy. less algunos síntomas comunes dificultad para caminar limitación del movimiento debilidad muscular en las piernas debilidad algunos diagnósticos relacionados 1 - 7 of 36 diagnósticos la neuropatía diabética neuropatía alcohólica la esclerosis múltiple ciática espondilolistesis miopatía alcohólica crónica distrofias musculares faja del miembro   más do i have 'atrofia muscular espinal tipo 4'? Además las siguientes pruebas de diagnóstico puede ser necesario para ayudar a verificar el diagnóstico: prueba de diagnóstico de los resultados de la búsqueda 'atrofia muscular espinal tipo 4' 1 - 5 of 16 pruebas de diagnóstico Los estudios genéticos moleculares atrofia muscular espinal tipo 4 y Los estudios genéticos moleculares La amniocentesis atrofia muscular espinal tipo 4 y La amniocentesis La gasometría arterial atrofia muscular espinal tipo 4 y La gasometría arterial Análisis de líquido cefalorraquídeo atrofia muscular espinal tipo 4 y Análisis de líquido cefalorraquídeo Ecocardiograma atrofia muscular espinal tipo 4 y Ecocardiograma ECG Electrocardiogram atrofia muscular espinal tipo 4 y ECG Electromiograma EMG atrofia muscular espinal tipo 4 y Electromiograma EMG Microscopía Electrónica atrofia muscular espinal tipo 4 y Microscopía Electrónica La biopsia muscular atrofia muscular espinal tipo 4 y La biopsia muscular Pruebas de función pulmonar atrofia muscular espinal tipo 4 y Pruebas de función pulmonar Oximetría de pulso Oximetry atrofia muscular espinal tipo 4 y Oximetría de pulso La creatina cinasa sérica de CK atrofia muscular espinal tipo 4 y La creatina cinasa sérica de CK Nervio NCS estudios de conducción atrofia muscular espinal tipo 4 y Nervio NCS estudios de conducción El monitoreo cardiaco atrofia muscular espinal tipo 4 y El monitoreo cardiaco Uretral catéter atrofia muscular espinal tipo 4 y Uretral catéter evocados motores de respuesta atrofia muscular espinal tipo 4 y evocados motores de respuesta para obtener más ingreso por favor, es de acceso libre (haga clic aquí para acceder) procedimientos terapéuticos para 'atrofia muscular espinal tipo 4'? La gestión o tratamiento de enfermedades debe ser siempre determinada por un proveedor de servicios de salud los pacientes. Abajo hay una lista de asociados procedimientos terapéuticos o medicamentos para spinal muscular atrophy type 4: resultados terapéuticos procedimiento de buscar 'atrofia muscular espinal tipo 4' 1 - 5 of 11 procedimientos terapéuticos clasificación son generadas por ordenador. por favor consulte a su proveedor de atención médica. Fisioterapia y Terapia Ocupacional Arthritis Physical and Occupational Therapy atrofia muscular espinal tipo 4 y Fisioterapia y Terapia Ocupacional Arriostre atrofia muscular espinal tipo 4 y Arriostre férula atrofia muscular espinal tipo 4 y férula Ortopedia Cuidado Quirúrgico atrofia muscular espinal tipo 4 y Ortopedia Cuidado Quirúrgico ortesis vertebral atrofia muscular espinal tipo 4 y ortesis vertebral Pecho de terapia física atrofia muscular espinal tipo 4 y Pecho de terapia física Sonda de Foley atrofia muscular espinal tipo 4 y Sonda de Foley Estimulación magnética transcraneal atrofia muscular espinal tipo 4 y Estimulación magnética transcraneal Uretral catéter atrofia muscular espinal tipo 4 y Uretral catéter de las vías aéreas atrofia muscular espinal tipo 4 y de las vías aéreas bastones y andadores atrofia muscular espinal tipo 4 y bastones y andadores para obtener más ingreso por favor, es de acceso libre (haga clic aquí para acceder) medicamentos para los resultados de la búsqueda 'atrofia muscular espinal tipo 4' clasificación son generadas por ordenador. por favor consulte a su proveedor de atención médica. resultados de la búsqueda web para atrofia muscular espinal tipo 4 Web (Todos)  |  Tratamiento  |  Droga  |  Pruebas  |  Investigación  |  Dieta Resultados 1 - 50 - atrofia muscular espinal tipo 4 Spinal Muscular Atrophy - Yahoo! Health [Traducir esta página] ... that the main title of the report Spinal Muscular Atrophy is not the name you expected. Please ... spinal muscular atrophy type 4 (SMA4) General Discussion ... http://health.yahoo.com/nervous-overview/spinal-muscular-atr...   health.yahoo.com - summary Spinal Muscular Atrophy [Traducir esta página] ... that the main title of the report Spinal Muscular Atrophy is not the name you expected. Please ... spinal muscular atrophy type 4 (SMA4) General Discussion ... http://www.webmd.com/brain/spinal-muscular-atrophy-11217   www.webmd.com - summary Spinal Muscular Atrophies: Peripheral Nervous System and Motor Unit ... [Traducir esta página] There are 4 main types. Type I spinal muscular atrophy (Werdnig-Hoffmann disease) is present in utero ... type II (intermediate) spinal muscular atrophy, ... http://www.merck.com/mmpe/print/sec16/ch223/ch223j.html   www.merck.com - summary Spinal Muscular Atrophy -- GeneReviews -- NCBI Bookshelf [Traducir esta página] ... of the presence of two SMN1 copies on one chromosome is 4 ... SPINAL MUSCULAR ATROPHY, TYPE IV; SMA4. 600354. SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1 ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sma   www.ncbi.nlm.nih.gov - summary MedlinePlus Medical Encyclopedia: Spinal muscular atrophy [Traducir esta página] Approximately 4 out of every 100,000 people have the condition. ... Infants with SMA type II have less severe symptoms during early infancy, but ... http://www.nlm.nih.gov/medlineplus/ency/article/000996.htm   www.nlm.nih.gov - summary Spinal muscular atrophy - Wikipedia, the free encyclopedia [Traducir esta página] Spinal Muscular Atrophy (SMA) is a term applied to a number of different ... Type 4: "Adult" 271150 [edit] SMA Caused by mutation of other genes ... http://en.wikipedia.org/wiki/Spinal_muscular_atrophy   en.wikipedia.org - summary Spinal muscular atrophy [Traducir esta página] ... to be affected) and has an incidence of approximately 4 per 100,000 people. In its most severe form (SMA type I, also called Werdnig-Hoffman disease) ... http://adam.about.com/encyclopedia/infectiousdiseases/Spinal...   adam.about.com - summary SPINAL MUSCULAR ATROPHY - INTERMEDIATE FORM - Pedbase.org [Traducir esta página] Type II - Intermediate Form (Intermediate) ... 4. Electrophysiological Studies. 1. EMG. evidence of denervation and reinnervation ... http://pedbase.org/s/spinal-muscular-atrophy_intermediate-form/   pedbase.org - summary Spinal Muscular Atrophy [Traducir esta página] Page 4. GeneReviews: Spinal Muscular Atrophy. GeneReviews ... SPINAL MUSCULAR ATROPHY, TYPE IV; SMA4. 600354. SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1 ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Spinal Muscular Atrophies: Peripheral Nerve Disorders: Merck Manual ... [Traducir esta página] In acute (type I) spinal muscular atrophy (Werdnig-Hoffmann disease), muscle ... the first year and in all by age 4 years, usually due to respiratory failure. ... http://www.merck.com/mmhe/au/print/sec06/ch095/ch095j.html   www.merck.com - summary Charcot-Marie-Tooth Neuropathy Type 2D/Distal Spinal Muscular Atrophy V [Traducir esta página] Page 4. GeneReviews: Charcot-Marie-Tooth Neuropathy Type 2D/Distal Spinal Muscular Atrophy V ... neuropathy type 2D/distal spinal muscular atrophy V (CMT2D/dSMA-V) ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Congenital heart defects in spinal muscular atrophy type I: a clinical ... [Traducir esta página] 1: Am J Med Genet A. 2008 Mar 15;146A(6):740-4. ... Spinal muscular atrophy type I (SMA I) was diagnosed by detecting a homozygous ... http://www.ncbi.nlm.nih.gov/pubmed/18266240?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary Neuromuscular Disorders - Genetics Home Reference [Traducir esta página] ... paraplegia type 2. spastic paraplegia type 3A. spastic paraplegia type 4. spastic paraplegia type 7. spinal and bulbar muscular atrophy. spinal muscular atrophy ... http://ghr.nlm.nih.gov/conditionGroup=neuromusculardisorders   ghr.nlm.nih.gov - summary Spinal Muscular Atrophy, X-Linked Infantile -- GeneReviews -- NCBI ... [Traducir esta página] ... with spinal muscular atrophy (pontocerebellar ... Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is ... 1995; 4: 1213?6. [PubMed] ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sma-xli   www.ncbi.nlm.nih.gov - summary Ministry Health Care [Traducir esta página] Spinal muscular atrophy (SMA) is a collection of different muscle diseases. ... Approximately 4 out of every 100,000 people have the condition. ... http://ministryhealth.adam.com/content.aspx?productId=101&pid=1&gid=000996   ministryhealth.adam.com - summary Characterization of spinal motor neuron loss in a mouse model of Spinal ... [Traducir esta página] Spinal Muscular Atrophy (SMA) is a neurodegenerative disease most commonly ... of the first lumbar segment at 4 days of age for both mutant and wild type mice. ... http://www.ninds.nih.gov/jobs_and_training/summer/2008_stude...   www.ninds.nih.gov - summary Spinal muscular atrophy: new thoughts on the pathogenesis and ... [Traducir esta página] ... collaborative study of spinal muscular atrophy, the second most common ... (type I or Werdnig-Hoffmann disease), whose life span is said to be only 2 to 4 ... http://www.ncbi.nlm.nih.gov/pubmed/1469240   www.ncbi.nlm.nih.gov - summary Spinal muscular atrophy type 1: A noninvasive respiratory management ... [Traducir esta página] 2000 Apr;117(4):1100-5. Comment in: Chest. 2002 Feb;121(2):665-6. Spinal muscular atrophy type 1: A noninvasive respiratory management approach. ... http://www.ncbi.nlm.nih.gov/pubmed/10767247   www.ncbi.nlm.nih.gov - summary Kennedy disease - Wikipedia, the free encyclopedia [Traducir esta página] Progressive proximal spinal and bulbar muscular atrophy of late onset. ... · X-linked agammaglobulinemia · Hyper-IgM syndrome type 1 · IPEX ... http://en.wikipedia.org/wiki/Spinobulbar_muscular_atrophy   en.wikipedia.org - summary WebMD Health A-Z - Find reliable health and medical information on ... [Traducir esta página] Spinal Muscular Atrophy Type I. Spinal Muscular Atrophy Type III ... 4. Salmonella FAQ. 5. Mariana Bridi da Costa. 6. Anxiety Drugs. 7. Patrick Swayze. 8 ... http://www.webmd.com/a-to-z-guides/health-topics/sp-st.htm   www.webmd.com - summary Brain and nervous system - Genetics Home Reference [Traducir esta página] ... Dominant Hereditary Spastic Paraplegia see spastic paraplegia type 4 ... spinal muscular atrophy, distal type V see distal hereditary motor neuropathy, type V ... http://www.ghr.nlm.nih.gov/conditionCategory=brainandnervoussystem   www.ghr.nlm.nih.gov - summary Charcot-Marie-Tooth disease - Genetics Home Reference [Traducir esta página] Type 4 and subtypes 2B1 and 2K are inherited in an autosomal recessive pattern, ... Review: Charcot-Marie-Tooth Neuropathy Type 2D/Distal Spinal Muscular Atrophy V ... http://ghr.nlm.nih.gov/condition=charcotmarietoothdisease   ghr.nlm.nih.gov - summary Werdnig Hoffman Disease - Yahoo! Health [Traducir esta página] Spinal Muscular Atrophy Type 1. Werdnig-Hoffman Paralysis. Disorder Subdivisions. None ... The different subtypes, SMA 0-4 are based on the age of onset of ... http://health.yahoo.com/nervous-overview/werdnig-hoffman-dis...   health.yahoo.com - summary MedlinePlus: Neuromuscular Disorders [Traducir esta página] Muscular dystrophy. Myasthenia gravis. Spinal muscular atrophy ... Genetics Home Reference: Spastic paraplegia type 4(National Library of Medicine) ... http://www.nlm.nih.gov/medlineplus/neuromusculardisorders.html   www.nlm.nih.gov - summary Spinal and Bulbar Muscular Atrophy [Traducir esta página] Page 4. GeneReviews: Spinal and Bulbar Muscular Atrophy. GeneReviews. GeneReviews. GeneReviews ... Type IV SMA, like SBMA, shows adult onset [Trentin et al 2005] ... http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...   www.ncbi.nlm.nih.gov - summary Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy ... [Traducir esta página] 1: Am J Med Genet A. 2004 Mar 15;125A(3):310-4. Erratum in: ... Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype. ... http://www.ncbi.nlm.nih.gov/pubmed/14994243   www.ncbi.nlm.nih.gov - summary Spinal and Bulbar Muscular Atrophy -- GeneReviews -- NCBI Bookshelf [Traducir esta página] Other forms of spinal muscular atrophy (SMA) that show ... Type IV SMA, like SBMA, shows adult onset [Trentin et al 2005] ... 1993; 43: 791?4. [PubMed] ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=kennedy   www.ncbi.nlm.nih.gov - summary Bones, muscles, and connective tissues - Genetics Home Reference [Traducir esta página] ... Hereditary Spastic Paraplegia see spastic paraplegia type 4 ... hereditary motor neuronopathy see spinal muscular atrophy. hereditary multiple exostoses ... http://ghr.nlm.nih.gov/ghr/conditionsByCategory/show/bonesmu...   ghr.nlm.nih.gov - summary A genetic and phenotypic analysis in Spanish spinal muscular atrophy ... [Traducir esta página] 2004 Apr;23(4):392-3. ... Spinal muscular atrophy (SMA) is an autosomal ... maximal motor milestones achieved in type I, II, and III (severe, intermediate, ... http://www.ncbi.nlm.nih.gov/pubmed/12872254   www.ncbi.nlm.nih.gov - summary A new mutation of IGHMBP2 gene in spinal muscular atrophy with ... [Traducir esta página] ... Pediatr Neurol. 2005 Apr;32(4):288-90. Comment in: Pediatr ... A new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1. ... http://www.ncbi.nlm.nih.gov/pubmed/15797190   www.ncbi.nlm.nih.gov - summary Spinal Muscular Atrophy Type 2 - Wikipedia, the free encyclopedia [Traducir esta página] Spinal Muscular Atrophy Type 2. From Wikipedia, the free encyclopedia ... 4 Source. 5 External links [edit] Symptoms. Children with spinal muscular atrophy ... http://en.wikipedia.org/wiki/Spinal_Muscular_Atrophy_Type_2   en.wikipedia.org - summary VAPB - VAMP (vesicle-associated membrane protein)-associated protein B ... [Traducir esta página] spinal muscular atrophy - caused by mutations in ... people with an adult-onset form of spinal muscular atrophy known as Finkel type. ... References (4 links) ... http://ghr.nlm.nih.gov/gene=vapb   ghr.nlm.nih.gov - summary Orphanet: Simple search [Traducir esta página] Molecular diagnosis of Proximal Spinal Muscular Atrophy, type 1, 2 and 3 (SMN1 gene) ... Molecular diagnosis of proximal spinal muscular atrophy type 1, 2, 3, 4 ... http://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simp...   www.orpha.net - summary 271150 [Traducir esta página] http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=271150   www.ncbi.nlm.nih.gov - summary Fiscal Year 2003 Budget Request: National Institute of Neurological ... [Traducir esta página] NINDS opening statement to the Congressional Subcommittees on Labor-HHS ... type 4, neurofibromatosis, reflex sympathetic dystrophy, spinal muscular atrophy, ... http://www.ninds.nih.gov/news_and_events/congressional_testi...   www.ninds.nih.gov - summary YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene ... [Traducir esta página] ... human RAB1 on Chr 2p13.4-p14 using somatic cell hybrids and ... neuromuscular disease, limb girdle muscular dystrophy type 2B, has been mapped to 2p13-p16. ... http://www.ncbi.nlm.nih.gov/pubmed/8838809   www.ncbi.nlm.nih.gov - summary Ramsay Hunt syndrome type I - Wikipedia, the free encyclopedia [Traducir esta página] 4 References. 5 External links [edit] Presentation ... Spinal muscular atrophy: Kennedy disease · spinal muscular atrophies of ... http://en.wikipedia.org/wiki/Ramsay_Hunt_syndrome_type_I   en.wikipedia.org - summary OMIM Update List for March, 2004 [Traducir esta página] 253400 SPINAL MUSCULAR ATROPHY, TYPE III; SMA3 ... 603935 PSORIASIS SUSCEPTIBILITY 4; PSORS4 ... 182970 SPINAL MUSCULAR ATROPHY, FACIOSCAPULOHUMERAL TYPE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2004   www.ncbi.nlm.nih.gov - summary Compensatory mechanisms during walking in response to muscle weakness ... [Traducir esta página] 1: Gait Posture. 2008 May;27(4):661-8. Epub 2007 Nov 5. ... of seven subjects with spinal muscular atrophy, type III (SMA group) and compare ... http://www.ncbi.nlm.nih.gov/pubmed/17980600?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary THE MERCK MANUAL OF GERIATRICS, Ch. 54, Muscular Disorders [Traducir esta página] Mild CK elevations (< 4 times the upper limit of the normal range) occur in some ... spinal canal narrowing) and other disorders that might produce muscular symptoms ... http://www.merck.com/mkgr/mmg/sec7/ch54/ch54a.jsp   www.merck.com - summary OMIM Update List for November, 1999 [Traducir esta página] 604320 SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1 ... 600759 ALZHEIMER DISEASE, FAMILIAL, TYPE 4. 600798 HERPESVIRUS ENTRY MEDIATOR B; HVEB ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.1999   www.ncbi.nlm.nih.gov - summary OMIM Update List for December, 1996 [Traducir esta página] 601011 CALCIUM CHANNEL, L TYPE, ALPHA-1 POLYPEPTIDE, ISOFORM 4; CACNL1A4 ... 600175 SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.1996   www.ncbi.nlm.nih.gov - summary OMIM Update List for April, 1996 [Traducir esta página] 182138 SOLUTE CARRIER FAMILY 6, MEMBER 4; SLC6A4. 217800 CORNEAL DYSTROPHY, MACULAR TYPE ... 253550 MUSCULAR ATROPHY, SPINAL, INTERMEDIATE TYPE; SMA II ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.1996   www.ncbi.nlm.nih.gov - summary Meningitis - Wikipedia, the free encyclopedia [Traducir esta página] ... influenzae type B (in areas without vaccination, see below).[1][4] In adults, ... paraplegia) · Spinal muscular atrophy: Werdnig-Hoffman · Kugelberg-Welander ... http://en.wikipedia.org/wiki/Spinal_meningitis   en.wikipedia.org - summary OMIM Update List for August, 2007 [Traducir esta página] 611067 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4; DSMA4 ... 253550 SPINAL MUSCULAR ATROPHY, TYPE II; SMA2. 271150 SPINAL MUSCULAR ATROPHY, TYPE IV; SMA4 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.2007   www.ncbi.nlm.nih.gov - summary Phenylbutyrate increases SMN expression in vitro: relevance for ... [Traducir esta página] Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease, ... with a highly variable phenotype ranging from very severe to mild (type I-III) ... http://www.ncbi.nlm.nih.gov/pubmed/14560316?ordinalpos=3&ito...   www.ncbi.nlm.nih.gov - summary Inherited motor neuron disease in domestic cats: a model of spinal ... [Traducir esta página] ... proximal muscle weakness, and muscle atrophy beginning at ~4 mo of age. ... similar to mild forms (type III) of spinal muscular atrophy in humans caused by ... http://www.ncbi.nlm.nih.gov/pubmed/15635053   www.ncbi.nlm.nih.gov - summary Werdnig-Hoffman disease - Wikipedia, the free encyclopedia [Traducir esta página] 4 Diagnosis. 5 Genetics. 6 Treatment. 7 Prognosis. 8 See also. 9 References ... Spinal muscular atrophy type 1: A noninvasive respiratory management approach" ... http://en.wikipedia.org/wiki/Werdnig-Hoffman_disease   en.wikipedia.org - summary National Institute of Neurological Disorders and Stroke (NINDS) [Traducir esta página] Part of the U.S. National Institutes of Health which conducts and supports research on brain and nervous system disorders. Site features background information, neurological disorder index, research laboratories, funding details, press releases, as well as training and career development opportunities for clinician scientists. http://www.ninds.nih.gov/   www.ninds.nih.gov - summary OMIM Update List for February, 1996 [Traducir esta página] 600759 ALZHEIMER DISEASE, FAMILIAL, TYPE 4; AD4. 600805 LAMININ, ALPHA 3; LAMA3. 600807 ASTHMA ... 253550 MUSCULAR ATROPHY, SPINAL, INTERMEDIATE TYPE; SMA II ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.1996   www.ncbi.nlm.nih.gov - summary mostrar más 1  2