Prions: Difference between revisions

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(Redirected page to Creutzfeld-Jakob disease)
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{| class="wikitable"
#REDIRECT [[Creutzfeld-Jakob disease]]
!Disease
!Abbr
!Host
!Etiology
|-
! colspan="4" |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
|-
! colspan="4" |Human Prion Diseases
|-
|Kuru
|—
|human
|ritualistic cannibalism
|-
|sporadic [[Creutzfeld-Jakob disease]]
|sCJD
|human
|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>
|-
|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 PrP<sup>C</sup> to PrP<sup>Sc</sup>
|-
|variably protease-sensitive prionopathy
|VPSPr
|human
|spontaneous mutation of PrP<sup>C</sup> to PrP<sup>Sc</sup>
|}
[[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