Literature DB >> 2938156

[Creutzfeldt-Jakob disease in France. Value of familial forms. Is there a gene controlling the length of the incubation period?].

F Cathala, P Brown, J Chatelain, P Castaigne, C Gajdusek.   

Abstract

An extensive search for patients who died of Creutzfeld-Jakob disease in France between 1968 and 1982 resulted in the discovery of 327 cases, 233 of which were histologically proven and 29 transmitted to animals; 17 patients belonged to 6 families. Further investigations among members of these 6 families yielded 21 additional cases, i.e. a total of 38 familial cases. Studies among sibships suggested an autosomal dominant pattern of transmission but did not exclude lateral contamination infancy. The patients' age at death was 10 to 15 years lower than that of the total of French cases and seemed to be a characteristic of each individual family. This suggests that, as in scrapie, a gene may control the length of the incubation period.

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Year:  1986        PMID: 2938156

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  2 in total

1.  Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors.

Authors:  R Harries-Jones; R Knight; R G Will; S Cousens; P G Smith; W B Matthews
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-09       Impact factor: 10.154

2.  Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.

Authors:  R Medori; H J Tritschler
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

  2 in total

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