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Creutzfeldt-jakob Disease as related to Brain Diseases


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CJD; Jakob-Creutzfeldt Disease; vCJD 

 

Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. Typically, onset of symptoms occurs at about age 60.. There are three major categories of CJD: sporadic CJD, hereditary CJD, and acquired CJD. There is currently no single diagnostic test for CJD. The first concern is to rule out treatable forms of dementia such as encephalitis or chronic meningitis. The only way to confirm a diagnosis of CJD is by brain biopsy or autopsy. In a brain biopsy, a neurosurgeon ...


Creutzfeldt-jakob Disease as related to Brain Diseases


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November 29, 2009


Page Updated: January 17, 2009
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