CJD Creutzfeldt-Jakob disease (CJD)a fatal neurodegenerative illness, is one form of familial spongiform encephalopathies (TSE) affecting humans. The suspected causal agent of these diseases is the priona proteinaceous infectious particle. Designated as PrPSC, this infectious protein is unique in that it does not contain nucleic acid, which is different from a virus, yet has the capability of government issue and being transmitted to other hosts. This capability of transmission poses a major problem in that the detection of the disease caused by this prion while the individual is in the incubation phase is not currently possible. Hence the disease may be well-timed transmitted to another individual through medical proceduresas seen in the quality study presented. Throughout the 20th century, sundry(a) case studies evolved and were compiled to form a sketchy descriptive invention for Creutzfeldt-Jakob disease. However, as time progressed, new forms of CJD emergedusua lly as ...If you require to condense a full essay, order it on our website: BestEssayCheap.com
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