MEDICAL DICTIONARY
Prion disease: A disease due to a prion , a proteinaceous infectious particle that lacks nucleic acids . Prions are composed largely, if not entirely, of an altered formal (an abnormal isoform) of a normal cellular protein . The known prion diseases of humans and other mammals are: - Bovine spongiform encephalopathy (BSE) -- also called mad cow disease; the natural hosts are cattle; the prion involved is the BSE prion.
- Creutzfeldt-Jakob disease (CJD) -- the natural hosts are humans; the prion involved is the CJD prion.
- Gerstmann-Sträussler-Scheinker syndrome (GSS) -- the natural hosts are humans; the prion involved is the GSS prion.
- Fatal familial insomnia (FFI) -- the natural hosts are humans; the prion involved is the FFI prion.
- Kuru -- the natural hosts are humans; the prion involved is the kuru prion.
- Scrapie -- the natural hosts of this disease are sheep and goats; the prion involved is the scrapie prion.
- Transmissible mink encephalopathy (TME) -- the natural hosts of this disease are mink; the prion involved is the TME prion.
- Chronic wasting disease (CWD) -- the natural hosts of this disease are mule deer, white-tailed deer, black-tailed deer, and elk; the prion involved is the CWD prion.
- Feline spongiform encephalopathy (FSE) -- the natural hosts are cats; the prion involved is the FSE prion.
- Exotic ungulate encephalopathy (EUE) -- the natural hosts are the nyala and greater kudu; the prion involved is the EUE prion.
See also: Prusiner, Stanley B. .
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