Prion disease is a transmittable condition that progressively impairs or destroys the nervous system. In humans, it presents as an acquired, familial through genetic inheritance and as a sporadic infection. The most common prion disease is Creutzfeldt-Jakob, which may be either inherited or sporadic. The global prevalence of the disease is documented as affecting one or two cases in a million people per year (Imran, 2011). The effects on the nervous system may result in symptoms such as hallucinations, fatigue memory loss and speech and movement difficulties (Parchi & Saverioni, 2012)
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