Prions: Difference between revisions
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(Redirected page to Creutzfeld-Jakob disease) Tags: New redirect Visual edit |
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{| class="wikitable" |
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⚫ | |||
!Disease |
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!Abbr |
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!Host |
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!Etiology |
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|- |
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! colspan="4" |Animal Prion Diseases |
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|- |
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|scrapie |
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|— |
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|ssheep and goats |
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|unknown origin |
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|- |
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|[[transmissible mink encephalopathy]] |
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|TME |
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|mink |
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|sheep or cattle origin |
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|- |
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|[[chronic wasting disease]] |
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|CWD |
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|cervids |
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|unknown origin |
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|- |
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|[[bovine spongiform encephalopathy]] |
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|BSE |
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|cattle |
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|unknown origin |
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|- |
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|[[exotic ungulate spongiform encephalopathy]] |
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|EUE |
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|Nyala, Kudu |
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|BSE origin |
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|- |
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|[[feline spongiform encephalopathy]] |
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|FSE |
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|cats |
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|BSE origin |
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|- |
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|[[non-human primate spongiform encephalopathy]] |
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|NHP |
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|lemurs |
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|BSE origin |
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|- |
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! colspan="4" |Human Prion Diseases |
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|- |
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|Kuru |
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|— |
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|human |
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|ritualistic cannibalism |
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|- |
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⚫ | |||
|sCJD |
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|human |
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|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup> |
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|- |
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|familial [[Creutzfeld-Jakob disease]] |
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|fCJD |
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|human |
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|mutations in PRNP gene |
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|- |
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|Gerstmann-Straüssler-Scheinker syndrome |
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|GSS |
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|human |
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|mutations in PRNP gene |
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|- |
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|iatrogenic [[Creutzfeld-Jakob disease]] |
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|iCJD |
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|human |
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|infection from surgical exposure to sCJD |
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|- |
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|fatal familial insomnia |
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|FFI |
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|human |
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|PRNP haplotype 178N-129M |
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|- |
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|variant [[Creutzfeld-Jakob disease]] |
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|vCJD |
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|human |
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|BSE origin |
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|- |
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|sporadic fatal insomnia |
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|sFI |
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|human |
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|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup> |
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|- |
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|variably protease-sensitive prionopathy |
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|VPSPr |
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|human |
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|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup> |
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|} |
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[[Category:Organisms]] |
Revision as of 01:50, 5 November 2020
Disease | Abbr | Host | Etiology |
---|---|---|---|
Animal Prion Diseases | |||
scrapie | — | ssheep and goats | unknown origin |
transmissible mink encephalopathy | TME | mink | sheep or cattle origin |
chronic wasting disease | CWD | cervids | unknown origin |
bovine spongiform encephalopathy | BSE | cattle | unknown origin |
exotic ungulate spongiform encephalopathy | EUE | Nyala, Kudu | BSE origin |
feline spongiform encephalopathy | FSE | cats | BSE origin |
non-human primate spongiform encephalopathy | NHP | lemurs | BSE origin |
Human Prion Diseases | |||
Kuru | — | human | ritualistic cannibalism |
sporadic Creutzfeld-Jakob disease | sCJD | human | spontaneous mutation of PrPC to PrPSc |
familial Creutzfeld-Jakob disease | fCJD | human | mutations in PRNP gene |
Gerstmann-Straüssler-Scheinker syndrome | GSS | human | mutations in PRNP gene |
iatrogenic Creutzfeld-Jakob disease | iCJD | human | infection from surgical exposure to sCJD |
fatal familial insomnia | FFI | human | PRNP haplotype 178N-129M |
variant Creutzfeld-Jakob disease | vCJD | human | BSE origin |
sporadic fatal insomnia | sFI | human | spontaneous mutation of PrPC to PrPSc |
variably protease-sensitive prionopathy | VPSPr | human | spontaneous mutation of PrPC to PrPSc |