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Cent Eur J Public Health. 2003
Mar;11(1):19-22. |
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Analysis of unusual
accumulation of Creutzfeldt-Jakob disease cases in Orava
and Liptov regions (northern Slovak focus) 1983-2000.
Mad'ar R, Maslenova D, Ranostajova K, Straka S, Baska T.
Institute of Epidemiology, Jessenius Faculty of
Medicine, Comenius University, Sklabinska 26, Martin,
037 53 Slovakia. MADAR@jfmed.uniba.sk
While familial cases of Creutzfeldt-Jakob disease are
extremely rare all over the world, 3 familial clusters
were observed between 1983-2000 in a relatively small
area situated in the North of Slovakia. Prevalence of
CJD in this area exceeded the overall prevalence in
Slovakia more than 8 times. The majority of CJD patients
admitted consuming sheep brain. Most patients lived in
small secluded villages with rather common familial
intermarriage. CJD affected both sexes equally. All
patients were prior to the disease mentally normal
individuals. Shortly after the onset of CJD their mental
status deteriorated remarkably with an average survival
rate of 3.6 months.
PMID: 12690798 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12690798&dopt=Abstract
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