Proteins and Prions
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What other prion diseases exist?
The following diseases are believed to be caused by prions.
In animals:
- Scrapie in sheep and goats
- Bovine spongiform encephalopathy (BSE) in cattle ("mad cow disease")
- Transmissible mink encephalopathy (TME) in mink
- Chronic wasting disease (CWD) in North American cervids (mule deer, white-tailed deer, elk and moose)
- Feline spongiform encephalopathy in cats
- Exotic ungulate encephalopathy (EUE) in nyala, oryx and greater kudu
In humans:
- Sporadic forms:
- Sporadic Creutzfeldt-Jakob disease (sCJD)
- Sporadic Fatal Insomnia (sFI)
- Genetic forms:
- Familial Creutzfeldt-Jakob disease (fCJD)
- Gerstmann-Sträussler-Scheinker syndrome (GSS)
- Fatal Familial Insomnia (FFI)
- Acquired forms:
- Iatrogenic Creutzfeldt-Jakob disease (iCJD)
- Variant Creutzfeldt-Jakob disease (vCJD)
- Kuru
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Prion_Normal_to_Abnormal.jpg
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