Mad Cow Disease - BSE: bovine TSE
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CJD: human TSE
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BSE was first observed in Great Britain in April, 1984, and was specifically diagnosed in 1986. Since 1986, nearly 200,000 cases of BSE in cattle have been identified in the United Kingdom. The epidemic peaked in 1992-93 at almost 1,000 cases per week. Control measures have reduced incidence and currently, less than 100 cases are being reported per week.
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Introduction:
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Description of spongiform encephalopathies, timeline and definition of terms |
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BSE:
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Signs, epidemiology, location, infectivity,
clinical tests relating to BSE |
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Prions:
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Prions are the causitive agent for
all TSEs Prion description, protein processing, structure, mutations, species differences, stability Prion transmission, transmission barriers, concerns Methods for identifying prion strains and tests |
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Human TSE:
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Description, causes and symptoms of human TSEs
including vCJD (nvCJD) |
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TSE of other species:
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Information of sheep scrapie and TSEs of cats, wild deer, elk, pets and mink |
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Other Information:
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Links to other BSE sites, to UIUC sites and to the authors |
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Slide Show: |
A set of 'slides' with information presented in a question and answer format. This section addresses many concerns relating ot BSE (Mad Cow Disease) in a straight-forward, unassuming manner. |
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Disclaimer: this site is designed as an outreach (extension) tool for the education of the general public regarding the risk, cause, concerns and problems associated with prion diseases in particular 'Mad Cow' disease. The authors are solely responsible for the content within this website and its interpretation. The information on human or animal TSEs should not be used as diagnostic tools; diagnosis of human or animal diseases can only be made by qualified medical doctors or veterinarians, respectively.
Copyright: The material within this website may be copied 'free of charge' for personal use. Permission to use material for other purposes should be requested from the University of Illinois at Urbana-Champaign via the website authors.
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