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Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal neurodegenerative disease. [ 4 ] [ 1 ] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances. [ 4 ]
Prion: No treatment and no cure [1] 100% [2] Includes Creutzfeldt–Jakob disease and all its variants, fatal insomnia, kuru, Gerstmann–Sträussler–Scheinker syndrome, Variably protease-sensitive prionopathy and others. [3] No cases of survival, invariably fatal. Rabies: Viral Unvaccinated ≈100% [4]
Fatal insomnia is an extremely rare neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom. [2] The majority of cases are familial (fatal familial insomnia [FFI]), stemming from a mutation in the PRNP gene, with the remainder of cases occurring sporadically (sporadic fatal insomnia [sFI]).
Also known as chronic wasting disease, "zombie deer disease" is a prion disease, a rare, progressive and fatal neurodegenerative disorder that affects deer, elk, moose and other animals, the CDC says.
Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, [1] ... (BSE or "mad cow disease") spread in cattle at an epidemic rate. The total ...
The CDC states that CWD is a prion disease or transmissible spongiform encephalopathy. Other TSEs include bovine spongiform encephalopathy or “mad cow disease” in cattle and scrapie in sheep ...
Gerstmann–Sträussler–Scheinker syndrome (GSS) is an extremely rare, always fatal (due to it being caused by prions) neurodegenerative disease that affects patients from 20 to 60 years in age. It is exclusively heritable, and is found in only a few families all over the world. [ 1 ]
Prion diseases occur when misfolded proteins cause normal proteins to misfold themselves by mechanisms yet unknown, thereby spreading disease. Misfolded proteins can accumulate into toxic clumps ...
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