Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance

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Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance.

Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disorder with a worldwide incidence of 1-1.5 per million. As in other countries, a CJD surveillance unit with a clinical and neuropathological approach was established in Goettingen (Germany) in 1993. Here we report the epidemiological data from a prospective 12-year surveillance. Since 1993, there has been an increasing inci...

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Creutzfeldt-Jakob disease: A case report

Background: Creutzfeldt-Jakob disease (CJD) as a life-threatening neurodegenerative disorder is not usually diagnosed in early stages of the disease because of a variety in its clinical manifestations. This study aimed to present a middle-aged woman with psychiatric symptoms who ultimately was diagnosed as a CJD case. Case presentation: This 48-year-old woman had progressive symptoms of depres...

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Creutzfeldt-Jakob disease (CJD) in humans and bovine spongiform encephalopathy (BSE) in cattle are subacute degenerative diseases of the brain classified as transmissible spongiform encephalopathies. BSE was first identified in 1986 in the United Kingdom (UK), where an epizootic involving > 155,000 cattle appeared to have been greatly amplified by exposure of calves to contaminated rendered cat...

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Creutzfeldt-Jakob disease surveillance and diagnosis.

Creutzfeldt-Jakob disease (CJD) and other transmissible spongiform encephalopa­ thies, also known as “prion diseases,” came to the world’s attention after the emergence of bovine spongiform enceph­ alopathy (BSE) in Europe and the sub­ sequent revelation of scientific evidence indicating that its transmission to humans causes a variant form of CJD [1]. Since BSE first emerged in the 1980s in th...

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ژورنال

عنوان ژورنال: Brain

سال: 2007

ISSN: 0006-8950,1460-2156

DOI: 10.1093/brain/awm063