Complete Androgen lnsensitivity Syndrome with 45,XY,t(13q;14q) Translocation (Two cases)

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Author(s)

    • OZDEMIR Ozturk
    • Department of Medixal Biology and Genetics, Faculty of Medicine, Cumhuriyet University
    • SUNGU Selma
    • Department of Medixal Biology and Genetics, Faculty of Medicine, Cumhuriyet University
    • PERCIN E. ferda
    • Department of Medixal Biology and Genetics, Faculty of Medicine, Cumhuriyet University
    • SEZGIN Llhan
    • Department of Medixal Biology and Genetics, Faculty of Medicine, Cumhuriyet University

Abstract

We report 2 cases of complete androgen insensitivity syndrome from 1 family with 45, XY, t(13q; 14q) karyotype including complete testicular feminisation (TF) clinical features. The chromosomal translocation is not generally considered part of the clinic spectrum in this group patients and most possibly it is the first report in the literature.

Journal

  • CYTOLOGIA

    CYTOLOGIA 67(2), 135-137, 2002-06-25

    Japan Mendel Society, International Society of Cytology

References:  10

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