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Sex Chromosomal Analysis of Spermatozoa from Infertile Men Using Fluorescence In Situ Hybridization

机译:荧光原位杂交技术对不育男性精子的性染色体分析

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摘要

>Purpose: To confirm an association between male infertilityand chromosome aberrations of spermatozoa, wedemonstrated the frequency of numerical abnormalities ofspermatozoa from infertile men with abnormal semen parameterscompared with fertile controls.>Method: Sperm cells from 10 infertile patients wereinvestigated for disomy rates of sex chromosomes and chromosome18 and diploidy by fluorescence in situ hybridization (FISH).All patients showed oligoasthenozoospermia with spermcounts 3–20 × 106/ml and motile rates 0–40%.>Results: Regarding XY disomy, a significantly higherfrequency was found in 8 of 10 patients as compared to normalfertile men. The disomy rates of chromosome 18, XX, YY,and diploidy rate were not increased.>Conclusions: There is an association between maleinfertility and embryo with aneuploidy of sex chromosomes.Counseling about possible genetic risks should be provided to theinfertile couples planning assisted reproduction treatment.
机译:>目的:为证实男性不育与精子染色体畸变之间的关系,我们证明了精子参数异常的不育男性与可育对照相比精子的数值异常发生率。>方法:通过荧光原位杂交(FISH)研究了10例不育患者的性染色体和18号染色体二倍体率和二倍体。所有患者均表现为少精子症,精子数为3–20×10 6 / ml,活动率为0– 40%。>结果:关于XY二体解剖,与正常可育男性相比,在10例患者中有8例的频率更高。 >结论:男性不育和胚胎与性染色体非整倍性之间存在相关性。应为可能的遗传风险提供咨询不孕夫妇计划辅助生殖治疗。

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