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Creutzfeldt-Jakob disease

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Creutzfeldt-Jakob disease: see prion prion , infectious agent thought to cause a group of diseases known as

prion diseases or transmissible spongiform encephalopathies. Well-known prion diseases are Creutzfeldt-Jakob disease (CJD) and kuru in humans, scrapie in sheep, bovine spongiform
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Creutzfeldt-Jakob disease

 or CJD

Rare fatal disease of the central nervous system. It destroys brain tissue, making it spongy and causing progressive loss of mental functioning and motor control. The disease commonly arises in adults between the ages of 40 and 70. Patients usually die within a year. There is no known cure. The disease is caused by a prion that builds up in neurons. Inherited or random mutation accounts for 99% of cases; the rest come from prion exposure during medical procedures and possibly from eating the meat of cattle with mad cow disease.



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Her son Andrew Black died of variant Creutzfeldt-Jakob Disease (vCJD) a year ago.
Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown cause.
If laboratory tests confirm the 64-year-old had Creutzfeldt-Jakob Disease (CJD), the human variant of bovine spongiform encephalopathy (BSE) or mad cow disease, it will be the fourth death from the disease in Spain.
 
 
 
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