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  • Hemofilije : klinika in opredelitev bolezni = Hemophilias : clinical features and diagnosis
    Andoljšek, Dušan
    Hemophilia is a group of hereditary diseases with different pathogenesis. Mutation of the gene located on chromosome X is their common feature. Consequently, protein synthesis, t.e. factor VIII and ... factor IX is disturbed. There may be a low protein level or an infunctional protein. Clinical featuresdepend only on the level of the functional protein and are the same infactor VIII and factor IX deficiency. laboratory investigation is necessary to differentiate both deficiencies. The structure of the factor IX and factor VIII gene has been recognised in the 70-ies and 80-ies. Since the prenatal diagnosis of hemophilia and carriers of the hemophilia can be recognised.
    Vir: Obzornik zdravstvene nege : strokovno glasilo Zveze društev medicinskih sester in zdravstvenih tehnikov Slovenije = journal of the Nurses Association of Slovenia. - ISSN 1318-2951 (Letn. 32, št. 3/4, 1998, str. 91-95)
    Vrsta gradiva - članek, sestavni del
    Leto - 1998
    Jezik - slovenski
    COBISS.SI-ID - 9127385

    Povezava(-e):

    Digitalna knjižnica Slovenije - dLib.si

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