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Home > Enfermedades Degenerativas: Ataxia de Friedreich, Enfermedad de Huntington, Esclerosis Multiple, Enfermedad de Creutzfeldt-Jakob(Spanish)
Enfermedades Degenerativas: Ataxia de Friedreich, Enfermedad de Huntington, Esclerosis Multiple, Enfermedad de Creutzfeldt-Jakob(Spanish)

Enfermedades Degenerativas: Ataxia de Friedreich, Enfermedad de Huntington, Esclerosis Multiple, Enfermedad de Creutzfeldt-Jakob(Spanish)

          
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About the Book

Fuente: Wikipedia. Paginas: 47. Capitulos: Ataxia de Friedreich, Enfermedad de Huntington, Esclerosis multiple, Enfermedad de Creutzfeldt-Jakob, Sindrome de Zellweger, Sindrome de Guillain-Barre, Enfermedad de Batten, Esclerosis lateral amiotrofica, Distrofia muscular de Duchenne, Neuromielitis optica, Incapacidad fisica, Sindrome de Wernicke-Korsakoff, Paralisis supranuclear progresiva, Encefalopatia espongiforme familiar asociada a una nueva mutacion en el gen PrP, Degeneracion macular asociada a la edad, Enfermedad de Lafora, Kuru, Miopatia, Enfermedad de Canavan, Sarcopenia, Sindrome de Korsakoff, Sindrome de Lowe, Distrofia muscular de Becker, Neurodegeneracion asociada a pantotenato quinasa, Sindrome de Stickler, Presbiacusia, Sindrome de Gerstmann-Straussler-Scheinker, Gliosis, Espondilosis, Enfermedad de Balo, Distrofia muscular congenita con deficit de merosina, Enfermedad degenerativa, Clinodactilia, Demencia cortical. Extracto: La enfermedad de Huntington (llamada tambien corea de Huntington y conocida antiguamente como baile de San Vito o mal de San Vito, al igual que otras coreas como la corea de Sydenham) es un trastorno genetico hereditario cuya consideracion clinica se puede resumir en que es un trastorno neuropsiquiatrico. Sus sintomas suelen aparecer hacia la mitad de la vida de la persona que lo padece (unos 30 o 50 anos de media) aunque pueden aparecer antes y los pacientes muestran degeneracion neuronal constante, progresiva e ininterrumpida hasta el final de la enfermedad que suele coincidir con el final de su vida por demencia y muerte o suicidio. Esta enfermedad genetica presenta una herencia autosomica dominante, lo cual significa que cualquier nino en una familia en la cual uno de los progenitores este afectado, tiene un 50% de probabilidades de heredar la mutacion que causa la enfermedad. El padecimiento de la enfermedad puede seguir caminos muy diferentes, incluso entre hermanos y parientes proximos. Esto se debe a que, junto a la mut...


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Product Details
  • ISBN-13: 9781231384831
  • Publisher: Books LLC, Wiki Series
  • Publisher Imprint: Books LLC, Wiki Series
  • Height: 246 mm
  • No of Pages: 48
  • Series Title: Spanish
  • Sub Title: Ataxia de Friedreich, Enfermedad de Huntington, Esclerosis Multiple, Enfermedad de Creutzfeldt-Jakob
  • Width: 189 mm
  • ISBN-10: 1231384832
  • Publisher Date: 02 Sep 2011
  • Binding: Paperback
  • Language: Spanish
  • Returnable: N
  • Spine Width: 3 mm
  • Weight: 104 gr


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