Bovine spongiform encephalopathy overview: Difference between revisions
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[[Category:Prions]] | |||
[[Category:Transmissible spongiform encephalopathies]] | |||
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Revision as of 19:12, 30 November 2012
Bovine Spongiform Encephalopathy Microchapters |
Differentiating Bovine Spongiform Encephalopathy from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Bovine spongiform encephalopathy overview On the Web |
American Roentgen Ray Society Images of Bovine spongiform encephalopathy overview |
Directions to Hospitals Treating Bovine spongiform encephalopathy |
Risk calculators and risk factors for Bovine spongiform encephalopathy overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Bovine spongiform encephalopathy is a transmissible spongiform encephalopathy of cattle associated with abnormal prion proteins in the brain. Affected animals develop excitability and salivation followed by ataxia. This disorder has been associated with consumption of scrapie infected ruminant derived protein. This condition may be transmitted to humans, where it is referred to as variant or new variant CREUTZFELDT-JAKOB SYNDROME.