Creutzfeldt-Jakob disease is a type of mental retardation that causes a quick decrease in movement and loss of psychological function. CJD is triggered by a protein called a prion. Domestic CJD occurs when a person inherits the abnormal prion from a parent; Acquired CJD consists of variant CJD, the kind pertaining to crazy cow disease. Iatrogenic CJD is additionally an acquired type of the disease. Iatrogenic CJD is occasionally passed with a blood product transfusion, transplant, or contaminated surgical instruments. Variant CJD is created by consuming infected meat. The infection that causes the disease in cows is believed to be the same one that causes vCJD in people. Most people with CJD will die within a year of the symptoms beginning, usually from infection. This is since the stability triggered by CJD can make people with the problem vulnerable to infection. The exact cause of erratic CJD is vague. Most cases of occasional CJD occur in adults aged between 45 and 75. Creutzfeldt-Jakob disease symptoms can be comparable to those of other dementia-like brain disorders, such as Alzheimer's disease. In people with the rarer vCJD, psychiatric symptoms might be more obvious at first. vCJD additionally influences people at a more youthful age and shows up to last 12 to 14 months.
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