All forms of CJD are caused by the presence of a faulty protein in the brain, called prion. Prions occur in both a normal form, which is a harmless protein found in the body's cells, and in an infectious form, which causes disease.
The causative agent of Creutzfeldt-Jakob disease is the CJD prion (proteinaceous infectous particle). It is neither virus, bacteria, protozoan or fungi. In fact, it is not living. It is a mutated...
CJD appears to affect males and females in equal numbers. It usually first appears in mid-life, beginning between ages 20 and 68, with the average age at onset of symptoms being around age 50.
Sporadic CJD, with no recognizable pattern of transmission, has an incidence of about one case per million people per year worldwide, making up 85% of total CJD cases, and 80% of all prion disease...