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

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

Pages
93–95
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

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.

📌 3 Key Takeaways

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Objective & Hypothesis: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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Key Findings & Data:Peripheral blood lymphocytes were cultured for chromosomal analysis and for each proband 30 metaphases were analyzed by GTG banding technique.
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Conclusion & Impact: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.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Male infertility · chromosomal abnormalities · Male infertility

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.

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.

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Cite This Article

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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