Literature DB >> 2253724

Familial Creutzfeldt-Jakob disease with temporal and spatial separation of affected members.

E Mitrova1, A Lowenthal, B Appeal.   

Abstract

Familial occurrence of three definitive and two possible cases of Creutzfeldt-Jakob disease (CJD) with temporal and spatial separation in the area of focal CJD accumulation in Slovakia is reported. Incubation period is 51 and 53 years respectively, if spatial and temporal separation of affected siblings is considered, and 51 years when the time interval between the death of the affected mother and the clinical onset in the first affected child is determined. Affected children tend to die at the same time (mean difference 3.3 years) and not at the same age (mean difference 6 years). Due to separation of the affected children, a possible common exposure to CJD infection was limited to approximately seven years during their childhood. Potential endo- and exogenous risk factors and a possible mode of CJD transmission in the described family, as well as in the CJD focus, is discussed.

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Year:  1990        PMID: 2253724     DOI: 10.1007/bf00150424

Source DB:  PubMed          Journal:  Eur J Epidemiol        ISSN: 0393-2990            Impact factor:   8.082


  11 in total

1.  Unconventional viruses and the origin and disappearance of kuru.

Authors:  D C Gajdusek
Journal:  Science       Date:  1977-09-02       Impact factor: 47.728

2.  Creutzfeldt-Jakob disease in Japan: an epidemiological study done in a select prefecture between 1976 and 1986.

Authors:  J Akai; O Ishihara; S Higuchi
Journal:  Neuroepidemiology       Date:  1989       Impact factor: 3.282

3.  Familial Creutzfeldt-Jakob disease.

Authors:  M Haltia; J Kovanen; H Van Crevel; G T Bots; S Stefanko
Journal:  J Neurol Sci       Date:  1979-08       Impact factor: 3.181

4.  Slow, latent and temperate virus infections of the central nervous system.

Authors:  D C Gajdusek; C J Gibbs
Journal:  Res Publ Assoc Res Nerv Ment Dis       Date:  1968

5.  Potential epidemic of Creutzfeldt-Jakob disease from human growth hormone therapy.

Authors:  P Brown; D C Gajdusek; C J Gibbs; D M Asher
Journal:  N Engl J Med       Date:  1985-09-19       Impact factor: 91.245

6.  [An analysis of cases of familial Creutzfeldt-Jakob disease in Slovakia].

Authors:  E Mitrová; L Czuhajová; E Gajdos; M Hovádová; A Nagy; J Rattaj
Journal:  Bratisl Lek Listy       Date:  1986-08       Impact factor: 1.278

7.  Bovine spongiform encephalopathy.

Authors:  T A Holt; J Phillips
Journal:  Br Med J (Clin Res Ed)       Date:  1988-06-04

8.  Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery.

Authors:  C Bernoulli; J Siegfried; G Baumgartner; F Regli; T Rabinowicz; D C Gajdusek; C J Gibbs
Journal:  Lancet       Date:  1977-02-26       Impact factor: 79.321

9.  Cluster of Creutzfeldt-Jakob disease and presenile dementia.

Authors:  V Mayer; D Orolin; E Mitrová
Journal:  Lancet       Date:  1977-07-30       Impact factor: 79.321

10.  The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature.

Authors:  P Brown; F Cathala; R F Raubertas; D C Gajdusek; P Castaigne
Journal:  Neurology       Date:  1987-06       Impact factor: 9.910

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  2 in total

1.  Some new aspects of CJD epidemiology in Slovakia.

Authors:  E Mitrová
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

2.  "Clusters" of CJD in Slovakia: the first statistically significant temporo-spatial accumulations of rural cases.

Authors:  E Mitrová; M Bronis
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

  2 in total

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