Creutzfeldt-Jakob disease (CJD) is an extremely rare degenerative brain disorder that is rapidly progressive, and usually, it leads to fatal complications and death within a year of onset of illness. Read more: How Do You Get Creutzfeldt-Jakob Disease? Article
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Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. CJD generally appears in the later years and runs a rapid course. Symptoms of CJD include failing memory, lack of coordination, visual disturbances, failing memory, blindness, weakness, and eventually coma. There are three major categories of CJD; 1) sporadic CJD, 2) hereditary CJD, and 3) acquired CJD. There is no cure for Creutzfeldt-Jakob disease.
Variant Creutzfeldt-Jakob Disease (vCJD)
Variant Creutzfeldt-Jakob disease (vCJD) is a degenerative, fatal brain disorder in humans. Symptoms are initially psychiatric or sensory and include neurological abnormalities such as ataxia, dementia, and myoclonus. There is no known treatment for vCJD.
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