Literature DB >> 3889706

High incidence of Creutzfeldt-Jakob disease in North African immigrants to France.

F Cathala, P Brown, P LeCanuet, D C Gajdusek.   

Abstract

During the 15-year period 1968-1982, 328 French residents died of Creutzfeldt-Jakob disease (CJD); 273 had been born in France (annual mortality rate of 0.38 per million inhabitants). Of the 55 foreign-born cases, 12 came from Tunisia and 11 from Algeria (mortality rates of 4.53 and 0.95 per million). Nearly all of the Tunisians were Jews, and six belonged to two families. These findings complement earlier observations on Libyan-born Israelis, but still do not discriminate between genetic or environmental causal factors, which will require epidemiologic investigation of CJD in North Africa.

Entities:  

Mesh:

Year:  1985        PMID: 3889706     DOI: 10.1212/wnl.35.6.894

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  Deletion in prion protein gene in a Moroccan family.

Authors:  J L Laplanche; J Chatelain; J M Launay; C Gazengel; M Vidaud
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

2.  A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986).

Authors:  C Masullo; M Pocchiari; G Neri; P Casaccia; A Iavarone; A Ladogana; G Macchi
Journal:  Eur J Epidemiol       Date:  1988-12       Impact factor: 8.082

Review 3.  The transmissible amyloidoses: genetical control of spontaneous generation of infectious amyloid proteins by nucleation of configurational change in host precursors: kuru-CJD-GSS-scrapie-BSE.

Authors:  D C Gajdusek
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.