Creutzfeldt-Jakob disease causes: Difference between revisions

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{{CMG}}
==Overview==
==Overview==
Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, invariably fatal neurodegenerative disorder believed to be caused by an abnormal isoform of a cellular glycoprotein known as the prion protein.<ref name="www.cdc.gov">{{Cite web  | last =  | first =  | title = http://www.cdc.gov/ncidod/dvrd/cjd/qa_cjd_infection_control.htm#what | url = http://www.cdc.gov/ncidod/dvrd/cjd/qa_cjd_infection_control.htm#what | publisher =  | date =  | accessdate = 14 February 2014 }}</ref>
Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, invariably fatal [[neurodegenerative disorder]] believed to be caused by an abnormal isoform of a cellular [[glycoprotein]] known as the prion protein.<ref name="www.cdc.gov">{{Cite web  | last =  | first =  | title = http://www.cdc.gov/ncidod/dvrd/cjd/qa_cjd_infection_control.htm#what | url = http://www.cdc.gov/ncidod/dvrd/cjd/qa_cjd_infection_control.htm#what | publisher =  | date =  | accessdate = 14 February 2014 }}</ref>


==Causes==
==Causes==

Revision as of 20:15, 29 June 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, invariably fatal neurodegenerative disorder believed to be caused by an abnormal isoform of a cellular glycoprotein known as the prion protein.[1]

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Human rabies virus immune globulin

References

  1. "http://www.cdc.gov/ncidod/dvrd/cjd/qa_cjd_infection_control.htm#what". Retrieved 14 February 2014. External link in |title= (help)

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