首页> 外文期刊>Human Genetics >Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient.
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Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient.

机译:估算47,XXY / 46,XY镶嵌Klinefelter患者的精子性别染色体二倍体和二倍体率。

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摘要

A 47,XXY/46,XY male was investigated for the incidence of aneuploidy in sperm sex chromosomes using a three-colour X/Y/18 fluorescence in situ hybridisation (FISH) protocol. A total of 1701 sperm nuclei were analysed. The ratio of X-bearing to Y-bearing sperm did not differ from the expected 1:1 ratio although there were more 23,Y sperm than 23,X sperm (844 vs 795). There was a significantly increased proportion of disomy XY and XX sperm compared with normal controls (0.41% vs 0.10%, P < 0.001 and 0.29% vs 0.04%, P < 0.01). However, the incidence of YY sperm was similar to the controls (0.06% vs 0.02%). The diploidy rate was also significantly increased (1.7% vs 0.13%, P < 0.0001), as was disomy 18 (0.71% vs 0.09%) and 25,XXY (0.47% vs 0%). The results support the hypothesis that some 47,XXY cells are able to undergo meiosis and produce mature spermatozoa. Patients with mosaic Klinefelter syndrome with severe oligozoospermia have significantly elevated incidences of disomy XY and XX sperm and may be at a slightly increased risk of producing 47,XXX and 47,XXY offspring. Additionally, they may be at risk of producing offspring with autosomal trisomies. Hence, patients with Klinefelter mosaicism scheduled for intracytoplasmic sperm injection intervention should first undergo FISH analysis of their sperm to determine their risk.
机译:使用三色X / Y / 18荧光原位杂交(FISH)方案,调查了47,XXY / 46,XY男性的精子性染色体中非整倍性的发生率。总共分析了1701个精子核。 X轴精子与Y轴精子的比例与预期的1:1比例没有差异,尽管23,Y精子比23,X精子多(844对795)。与正常对照组相比,XY和XX精子二体比例显着增加(0.41%vs 0.10%,P <0.001和0.29%vs 0.04%,P <0.01)。但是,YY精子的发生率与对照组相似(0.06%对0.02%)。二倍体率也显着提高(1.7%vs 0.13%,P <0.0001),二体性18(0.71%vs 0.09%)和25,XXY(0.47%vs 0%)也是如此。结果支持以下假设:一些47,XXY细胞能够进行减数分裂并产生成熟的精子。患有严重少精症的镶嵌Klinefelter综合征患者的XY和XX精子二体性发病率显着升高,并且产生47,XXX和47,XXY后代的风险可能会略有增加。此外,他们可能有产生常染色体三体性的后代的风险。因此,计划进行胞浆内单精子注射干预的克氏综合征患者应首先对其精子进行FISH分析以确定其风险。

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