Difference between revisions of "Creutzfeldt-Jakob Disease"
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| − | + | '''Creutzfeldt-Jacob Disease''' is a sporadic and rare, but fatal human [[disease]] that usually strikes people over 65. It occurs worldwide at an estimated rate of one case per million population. About 10-15% of CJD cases are inherited. A small number of cases occurred as the result of various medical treatments or procedures which inadvertently transferred the CJD agent. In March 1996, the British government announced a possible link between bovine spongiform encephalopathy (BSE) and CJD. The announcement was prompted by the discovery of several atypical cases of CJD in Great Britain. | |
==References== | ==References== | ||
[http://www.fsis.usda.gov/Help/A-Z_Index/index.asp USDA Index] | [http://www.fsis.usda.gov/Help/A-Z_Index/index.asp USDA Index] | ||
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| + | [[Category:Diseases]] | ||
Revision as of 07:31, November 14, 2007
Creutzfeldt-Jacob Disease is a sporadic and rare, but fatal human disease that usually strikes people over 65. It occurs worldwide at an estimated rate of one case per million population. About 10-15% of CJD cases are inherited. A small number of cases occurred as the result of various medical treatments or procedures which inadvertently transferred the CJD agent. In March 1996, the British government announced a possible link between bovine spongiform encephalopathy (BSE) and CJD. The announcement was prompted by the discovery of several atypical cases of CJD in Great Britain.