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Ceutzfeldt-Jakob Disease Research Paper

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Ceutzfeldt-Jakob disease (CJD) refers to a rare but very deadly brain disorder. In early stages, the patient may experience memory impairment, visual difficulties, behavioral issues and poor coordination of body parts. At developed stages, the patients experience involuntary body movement, mental disability, extreme body weakness and coma. The disease is divided into three main categories namely; sporadic, hereditary and Acquired CJD. The risk factors for sporadic CJD are not known though it is the most common type of the CJD. For hereditary CJD, the patient inherits the disease from genetically close family members such as biological parents. On the other hand, the patient is infected with Acquired CJD as a result of exposure of nervous tissues.

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