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[男性不育的染色体研究]

[Chromosomal studies of male infertility].

作者信息

Kalantari P, Sepehri H, Behjati F, Ashtiani Z Ousati, Akbari M T

机构信息

College of Biology, Tehran University, Tehran 19916, Iran. pkalantari(8)vahoo.com

出版信息

Genetika. 2003 Mar;39(3):423-6.

Abstract

Prometaphase and metaphase chromosome analyses performed on 70 consecutive men with primary infertility (for a period of at least 2 years) revealed 8 (11.42%) men with some kind of chromosomal abnormality. The highest frequency of abnormal karyotypes (10%) was found among patients with azpospennia and the most frequent anomaly was 47, XXY chromosomal constitution, found in 6 (8.57%) patients. All the chromosomal aberrations found in this study was sex chromosomal type and we did not find any autosomal aberration. All patients with numerical chromosomal anomalies had azoospermia. The incidence of structural aberration in our study was 1.42%. Fifteen patients had different chromosomal variants (21.38%). We suggest that men with azoospermia should be considered for cytogenetic investigation and we report that "variants of the Y chromosome" have no influence on the sperm count (million/ml) and fertility of men.

摘要

对70名连续的原发性不育男性(不育时间至少2年)进行前中期和中期染色体分析,发现8名(11.42%)男性存在某种染色体异常。在无精子症患者中发现异常核型的频率最高(10%),最常见的异常是47, XXY染色体组成,在6名(8.57%)患者中发现。本研究中发现的所有染色体畸变均为性染色体类型,未发现任何常染色体畸变。所有染色体数目异常的患者均为无精子症。本研究中结构畸变的发生率为1.42%。15名患者有不同的染色体变异(21.38%)。我们建议对无精子症男性进行细胞遗传学检查,并且我们报告“Y染色体变异”对男性的精子计数(百万/毫升)和生育能力没有影响。

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