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一名患有中度少弱畸精子症的46,XY/45,X嵌合型男性的体细胞和精子的细胞遗传学

Cytogenetics of somatic cells and sperm from a 46,XY/45,X mosaic male with moderate oligoasthenoteratozoospermia.

作者信息

Newberg M T, Francisco R G, Pang M G, Brugo S, Doncel G F, Acosta A A, Hoegerman S F, Kearns W G

机构信息

Center for Pediatric Research, Eastern Virginia Medical School, Norfolk 23510, USA.

出版信息

Fertil Steril. 1998 Jan;69(1):146-8. doi: 10.1016/s0015-0282(97)00443-3.

Abstract

OBJECTIVE

To determine aneuploidy frequencies in sperm from a patient with normal phenotype and 46,XY/45,X mosaicism in somatic cells (peripheral lymphocytes).

DESIGN

Case report.

SETTING

Infertility clinic and genetics laboratory.

PATIENT

A 30-year-old male with primary infertility and moderate oligoasthenoteratozoospermia.

INTERVENTION(S): Cytogenetic analysis of somatic cells and determination by fluorescence in situ hybridization of aneuploidy frequencies for the gonosomes (sex chromosomes) and chromosome 18 in sperm from whole and Percoll-separated semen.

MAIN OUTCOME MEASURE(S): Somatic and gametic aneuploidy were scored.

RESULT(S): Analysis of lymphocyte metaphase cells showed a mosaic 46,XY (90%)/ 45,X (10%) karyotype. Significantly higher frequencies of gonosomal (semen, 1.92% versus 0.70%; Percoll, 1.12% versus 0.46%), and chromosome 18 (semen, 0.89% versus 0.28%; Percoll, 0.26% versus 0.10%) disomy were detected in the sperm of the patient compared with those observed in spermatozoa from a proved fertile control.

CONCLUSION(S): Significantly higher frequencies of aneuploid sperm suggest that the patient is at elevated risk of producing offspring with numerical chromosome abnormalities.

摘要

目的

确定一名体细胞(外周血淋巴细胞)表型正常且存在46,XY/45,X嵌合体的患者精子中的非整倍体频率。

设计

病例报告。

地点

不孕不育诊所和遗传学实验室。

患者

一名30岁男性,原发性不孕,伴有中度少弱畸精子症。

干预措施

对体细胞进行细胞遗传学分析,并通过荧光原位杂交测定全精液和经Percoll分离精液中精子的性染色体(性腺染色体)和18号染色体的非整倍体频率。

主要观察指标

对体细胞和配子的非整倍体进行评分。

结果

淋巴细胞中期细胞分析显示为46,XY(90%)/45,X(10%)的嵌合核型。与经证实可育的对照者精子相比,该患者精子中性染色体(精液中为1.92%对0.70%;Percoll分离精液中为1.12%对0.46%)和18号染色体(精液中为0.89%对0.28%;Percoll分离精液中为0.26%对0.10%)的二体频率显著更高。

结论

非整倍体精子的频率显著更高,提示该患者生育染色体数目异常后代的风险增加。

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