viernes, 8 de junio de 2012

Creutzfeldt-Jakob Disease: MedlinePlus [NEW TOPIC PAGE]

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Creutzfeldt-Jakob Disease: MedlinePlus

 
A service of the U.S. National Library of Medicine
From the National Institutes of HealthNational Institutes of Health


05/31/2012 08:00 PM EDT

Source: Dept. of Agriculture
05/31/2012 08:00 PM EDT

Source: Food and Drug Administration - PDF

Creutzfeldt-Jakob Disease

Also called: CJD 
 
 
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative brain disorder. Symptoms usually start around age 60. Memory problems, behavior changes, vision problems and poor muscle coordination progress quickly to dementia, coma and death. Most patients die within a year.
The three main categories of CJD are
  • sporadic CJD, which occurs for no known reason
  • hereditary CJD, which runs in families
  • acquired CJD, which occurs from contact with infected tissue, usually during a medical procedure
Cattle can get a disease related to CJD called bovine spongiform encephalopathy (BSE) or "mad cow disease." There is concern that people can get a variant of CJD from eating beef from an infected animal, but there is no direct proof to support this.
NIH: National Institute of Neurological Disorders and Stroke

Illustration of the brain

MEDICAL ENCYCLOPEDIA  

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