Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases

After a cluster of Creutzfeldt-Jakob disease (CJD) cases among unusually young patients was reported recently from the United Kingdom, we examined trends and the current incidence of CJD in the United States. We found that the age-adjusted CJD death rate in the United States is similar to published...

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Main Authors: Robert C. Holman, Ali S. Khan, Ermias D. Belay, Lawrence B. Schonberger
Format: Article
Language:English
Published: Centers for Disease Control and Prevention 1996-10-01
Series:Emerging Infectious Diseases
Subjects:
Online Access:https://wwwnc.cdc.gov/eid/article/2/4/96-0409_article
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author Robert C. Holman
Ali S. Khan
Ermias D. Belay
Lawrence B. Schonberger
author_facet Robert C. Holman
Ali S. Khan
Ermias D. Belay
Lawrence B. Schonberger
author_sort Robert C. Holman
collection DOAJ
description After a cluster of Creutzfeldt-Jakob disease (CJD) cases among unusually young patients was reported recently from the United Kingdom, we examined trends and the current incidence of CJD in the United States. We found that the age-adjusted CJD death rate in the United States is similar to published estimates of the crude incidence of CJD worldwide and has continued to be stable from 1979 through 1994. The number of CJD deaths in persons <45 years of age remained stable during this period. We found no evidence of the variant form of CJD.
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spelling doaj.art-c42dfcdc33b84de5bc6c9e6d419860242022-12-22T00:51:22ZengCenters for Disease Control and PreventionEmerging Infectious Diseases1080-60401080-60591996-10-012433333710.3201/eid0204.960409Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant CasesRobert C. HolmanAli S. KhanErmias D. BelayLawrence B. SchonbergerAfter a cluster of Creutzfeldt-Jakob disease (CJD) cases among unusually young patients was reported recently from the United Kingdom, we examined trends and the current incidence of CJD in the United States. We found that the age-adjusted CJD death rate in the United States is similar to published estimates of the crude incidence of CJD worldwide and has continued to be stable from 1979 through 1994. The number of CJD deaths in persons <45 years of age remained stable during this period. We found no evidence of the variant form of CJD.https://wwwnc.cdc.gov/eid/article/2/4/96-0409_articleUnited States
spellingShingle Robert C. Holman
Ali S. Khan
Ermias D. Belay
Lawrence B. Schonberger
Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases
Emerging Infectious Diseases
United States
title Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases
title_full Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases
title_fullStr Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases
title_full_unstemmed Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases
title_short Creutzfeldt-Jakob Disease in the United States, 1979-1994: Using National Mortality Data to Assess the Possible Occurrence of Variant Cases
title_sort creutzfeldt jakob disease in the united states 1979 1994 using national mortality data to assess the possible occurrence of variant cases
topic United States
url https://wwwnc.cdc.gov/eid/article/2/4/96-0409_article
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