Dergiler / Turkish Journal of Medical Sciences / 1998 / Cilt: 28 - Sayı: 1

The Frequency of Chromosomal Abnormalities in Men With Azoospermia and Oligoasthenoteratozoospermia: a Preliminary Study

Sayfa
93–95
Yayın Tarihi
2022-11-05
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

As prenatal diagnosis is indicated if an infertle man with an abnormal karyotype fathers a child, it is particularly important to know this fact before providing infertility treatment.

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Amaç & Hipotez:The aim of this study is to investigate the frequency of chromosomal abnormalities in men with severe andrological infertility, In 50 men with azoospermia and severe oligoasthenoteratozoospermia (OAT), who referred for our intracytoplasmic sperm injection program, a cytogenetic study has been prospectively carried out.
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Temel Bulgular & Veri:Peripheral blood lymphocytes were cultured for chromosomal analysis and for each proband 30 metaphases were analyzed by GTG banding technique.
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Sonuç & Katkı:As prenatal diagnosis is indicated if an infertle man with an abnormal karyotype fathers a child, it is particularly important to know this fact before providing infertility treatment.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Male infertility · chromosomal abnormalities · Male infertility

Özet

The aim of this study is to investigate the frequency of chromosomal abnormalities in men with severe andrological infertility, In 50 men with azoospermia and severe oligoasthenoteratozoospermia (OAT), who referred for our intracytoplasmic sperm injection program, a cytogenetic study has been prospectively carried out. Peripheral blood lymphocytes were cultured for chromosomal analysis and for each proband 30 metaphases were analyzed by GTG banding technique. Major chromosomal abnormalities were detected in 4 of cases (8%). There were 3 sex-chromosome abnormalities, 46XXY in all 3 cases, and one autosomal chromosomal abnormality 46 XY, t (1;7) (P32;Q32). Although the sample size is small, the high frequency of chromosomal abnormalities detected in this preliminary study emphasizes the importance of chromosomal analysis in subfertile men. As prenatal diagnosis is indicated if an infertle man with an abnormal karyotype fathers a child, it is particularly important to know this fact before providing infertility treatment.

Abstract

The aim of this study is to investigate the frequency of chromosomal abnormalities in men with severe andrological infertility, In 50 men with azoospermia and severe oligoasthenoteratozoospermia (OAT), who referred for our intracytoplasmic sperm injection program, a cytogenetic study has been prospectively carried out. Peripheral blood lymphocytes were cultured for chromosomal analysis and for each proband 30 metaphases were analyzed by GTG banding technique. Major chromosomal abnormalities were detected in 4 of cases (8%). There were 3 sex-chromosome abnormalities, 46XXY in all 3 cases, and one autosomal chromosomal abnormality 46 XY, t (1;7) (P32;Q32). Although the sample size is small, the high frequency of chromosomal abnormalities detected in this preliminary study emphasizes the importance of chromosomal analysis in subfertile men. As prenatal diagnosis is indicated if an infertle man with an abnormal karyotype fathers a child, it is particularly important to know this fact before providing infertility treatment.

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Bu Makaleye Atıf Yap

TÜZÜN, C., KAHRAMAN, S., IŞIK, A. Z., VİCDAN, K., ÖZGÜR, S., BİBEROĞLU, K. (2022). The Frequency of Chromosomal Abnormalities in Men With Azoospermia and Oligoasthenoteratozoospermia: a Preliminary Study. Turkish Journal of Medical Sciences, Cilt: 28 - Sayı: 1, 93–95. https://ajindex.com/articles/612642

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