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  1. Cystic fibrosis carrier frequencies in populations of African origin.

    Article - En anglais

    Cystic fibrosis (CF) is a common autosomal recessive disorder in populations of European descent.

    However, very little is known about CF in populations of African origin among whom it has been believed to be extremely rare.

    The aim of this study was to determine if this is the case or whether it is under-reported.

    A CFTR mutation, 3120+1G-A, which was first reported in three African-American CF patients, has been shown to account for 9-14% of African-American CF chromosomes.

    It has also been found in 4/6 CF chromosomes in South African blacks and one CF chromosome of Cameroonian origin.

    In order to determine the carrier frequency of the 3120+1G-A mutation in Africa, 1360 unrelated, healthy subjects were screened.

    Nine carriers were identified.

    In addition, two out of five black CF patients with positive sweat tests were found to be heterozygous for the 3120+1G-A mutation and two out of another four black patients with symptoms suggestive of CF, but unconfirmed by sweat tests, were heterozygous for the D1270N mutation.

    A further three CFTR mutations, A559T, S1255X, and 444de1A, which had been found in African-American CF patients, were not identified in the patients or in over 373 healthy subjects tested.

    The 3120+1G-A mutation has a carrier frequency of 1 in 91 (8/728) in South African blacks with a 95% confidence interval of 1 in 46 to 1 in 197. (...)

    Mots-clés Pascal : Mucoviscidose, Porteur, Fréquence génique, Homme, Ethnie, Négroïde, Mutation, Gène, Incidence, Hétérozygotie, Dépistage, Exploration, Appareil respiratoire pathologie, Appareil digestif pathologie, Pancréas pathologie, Maladie héréditaire, Métabolisme pathologie

    Mots-clés Pascal anglais : Cystic fibrosis, Carrier, Gene frequency, Human, Ethnic group, Negroid, Mutation, Gene, Incidence, Heterozygosity, Medical screening, Exploration, Respiratory disease, Digestive diseases, Pancreatic disease, Genetic disease, Metabolic diseases

    Logo du centre Notice produite par :
    Inist-CNRS - Institut de l'Information Scientifique et Technique

    Cote : 99-0094935

    Code Inist : 002B13C03. Création : 31/05/1999.