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两名患有无精子症的正常健康男性中的嵌合环状Y染色体。

Mosaic ring Y chromosome in two normal healthy men with azoospermia.

作者信息

Bertini Veronica, Canale Domenico, Bicocchi Maria Patrizia, Simi Paolo, Valetto Angelo

机构信息

Laboratory of Cytogenetics and Molecular Genetics, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

出版信息

Fertil Steril. 2005 Dec;84(6):1744. doi: 10.1016/j.fertnstert.2005.06.034.

Abstract

OBJECTIVE

To better define by molecular and cytogenetic techniques ring Y chromosomes detected in 2 infertile men.

DESIGN

Case report.

SETTING

Molecular genetics/cytogenetics unit in a university hospital.

PATIENT(S): Two infertile men with azoospermia, presenting a normal male phenotype with complete masculinization.

INTERVENTION(S): Karyotype and genetic counseling.

MAIN OUTCOME MEASURE(S): Metaphases were studied by standard G- and Q-banding; fluorescent in situ hybridization and PCR were performed to analyze specific Y chromosome regions.

RESULT(S): Chromosomal analysis detected a mosaicism with a Y chromosome ring cell line in 92% (patient 1) and 95% (patient 2) of the metaphases, coexisting with a 45,X cell line in the remaining metaphases. In patient 1, PCR analysis showed the presence of AZFa region and a partial deletion of AZFb region; AZFc region was deleted. In patient 2 all three AZF regions were deleted.

CONCLUSION(S): A 45,X/46,X,r(Y) mosaicism can be detected not only in patients with Ullrich-Turner syndrome and in patients with various degrees of genital ambiguity but also in men presenting a normal phenotype. Their azoospermia can be explained by partial or total deletion of AZF regions.

摘要

目的

运用分子和细胞遗传学技术更准确地界定在两名不育男性中检测到的环状Y染色体。

设计

病例报告。

地点

大学医院的分子遗传学/细胞遗传学科室。

患者

两名无精子症的不育男性,表现为具有完全男性化特征的正常男性表型。

干预措施

核型分析和遗传咨询。

主要观察指标

通过标准G显带和Q显带研究中期分裂相;进行荧光原位杂交和聚合酶链反应以分析特定的Y染色体区域。

结果

染色体分析在92%(患者1)和95%(患者2)的中期分裂相中检测到含有Y染色体环状细胞系的嵌合体,其余中期分裂相中并存有45,X细胞系。在患者1中,聚合酶链反应分析显示存在AZFa区域以及AZFb区域的部分缺失;AZFc区域缺失。在患者2中,所有三个AZF区域均缺失。

结论

不仅在患有乌尔里希-特纳综合征的患者以及具有不同程度生殖器模糊的患者中可检测到45,X/46,X,r(Y)嵌合体,在表现为正常表型的男性中也可检测到。他们的无精子症可通过AZF区域的部分或全部缺失来解释。

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