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Volume : 36 Issue : 3 Year : 2021



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Oligoasthenozoospermia with rare karyotype [Medeniyet Med J]
Medeniyet Med J. 2007; 22(4): 158-160

Oligoasthenozoospermia with rare karyotype

Ülkü Özbey, Hüseyin Yüce
Firat University Faculty of Medicine, Department of Medical Biology and Genetics, Elazig

In a couple who had been investigated because of infertility, oligo-asthenozoospermia was diagnosed in man, by sperm analysis. Cytogenetic analyse, the karyotype of man was exhibited as 46,XY, t(9;15) (pter ›q21.1: : q11.1›qter), der(9)(ptel›q21.1), whereas his wife's was 46,XX. To our knowlodge, this is the first case, which was determined by conventional cytogenetic techniques, reported in the literature associated with severe male infertility. The degree of the efficiency of this rare karyotype on abortions and genetic counselling period that includes evaluating the view of unbalanced segragations of this karyotype was argued based on the literature.

Keywords: Male infertility, chromosomal translocation, Oligoasthenozoospermia, meiotic pattern


Nadir karyotipli oligoastenozoospermi

Ülkü Özbey, Hüseyin Yüce
Fırat Üniversitesi Tıp Fakültesi, Tıbbi Biyoloji ve Genetik Anabilim Dalı, Elazığ

Anahtar Kelimeler: Erkek infertilitesi, kromozomal translokasyon, oligoastenozoospermi, mayotik patern


Ülkü Özbey, Hüseyin Yüce. Oligoasthenozoospermia with rare karyotype. Medeniyet Med J. 2007; 22(4): 158-160

Corresponding Author: Ülkü Özbey, Türkiye


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