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The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation.
Chapman, J; Ben-Israel, J; Goldhammer, Y; Korczyn, A D.
Afiliación
  • Chapman J; Department of Neurology, Tel Aviv Medical Center, Israel.
Neurology ; 44(9): 1683-6, 1994 Sep.
Article en En | MEDLINE | ID: mdl-7936296
We determined the penetrance of the PRNP 200Lys mutation in the large cluster of Creutzfeldt-Jakob disease (CJD) cases among Jews of Libyan-Tunisian origin living in Israel, utilizing data from 52 carriers with definite or probable CJD and 34 unaffected mutation carriers. A life table analysis was carried out with development of CJD as the end point. The probability of developing CJD rose with age, fitting a second-order regression curve (R = 0.97, p < 0.001). The cumulative penetrance reached 50% at the age of 60 and 80% at 80 years. Including seven elderly possible CJD patients in the analysis made the penetrance approach 100% by age eighty. The penetrance of the mutation is high, and although age is a predominant influencing factor, other factors, such as gender, may also play a role.
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Base de datos: MEDLINE Asunto principal: Priones / Síndrome de Creutzfeldt-Jakob / Mutación Puntual Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Africa / Asia Idioma: En Revista: Neurology Año: 1994 Tipo del documento: Article País de afiliación: Israel
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Base de datos: MEDLINE Asunto principal: Priones / Síndrome de Creutzfeldt-Jakob / Mutación Puntual Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Africa / Asia Idioma: En Revista: Neurology Año: 1994 Tipo del documento: Article País de afiliación: Israel