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46,XY,t(3;6)(p24;p21.2),inv(8)(p11;2q21.2) 双重染色体重排患者的精子 FISH 分析。

Sperm FISH analysis of a 46,XY,t(3;6)(p24;p21.2),inv (8)(p11;2q21.2) double chromosomal rearrangement.

机构信息

Department of Reproductive Biology, Cytogenetics, Gynaecology and Obstetrics, CHIPS, Poissy, France.

出版信息

Reprod Biomed Online. 2012 Feb;24(2):219-23. doi: 10.1016/j.rbmo.2011.10.009. Epub 2011 Oct 25.

DOI:10.1016/j.rbmo.2011.10.009
PMID:22196892
Abstract

A complex chromosome rearrangement (CCR) can be defined as a structural chromosomal aberration that involves at least three breakpoints located on two or more chromosomes. Highly unbalanced gametes may lead to infertility or congenital malformations. Here is reported a double rearrangement considered as the simplest possible CCR and, in a sense, not a true CCR, meiotic segregation for a 46,XY,t(3;6)(p24;p21.2),inv(8)(p11;2q21.2) male patient referred after his partner had undergone three early miscarriages. Sperm fluorescence in-situ hybridization was used to screen for translocation and inversion segregation and an interchromosomal effect (ICE) for 13 chromosomes not involved in CCR. The malsegregation rates for the reciprocal translocation and pericentric inversion were 61.2% and 1.7%, respectively. ICE analysis revealed that the observed chromosome aneuploidy rates of between 0.1% and 0.8% did not differ significantly from control values. A slight increase in cumulative ICE (P=0.049) was observed in the patient, relative to control spermatozoa (with rates of 4.6% and 3.1%). The sperm DNA fragmentation rate differed significantly from control values (5.0%; P=0.001). Reciprocal translocation had no impact on meiotic segregation of the pericentric inversion in this double rearrangement. No conclusion could be drawn regarding the impact of pericentric inversion on translocation.

摘要

一种复杂的染色体重排(CCR)可以定义为一种结构染色体异常,涉及至少三个断点,位于两个或更多染色体上。高度不平衡的配子可能导致不孕或先天畸形。这里报告了一个双重重排,被认为是最简单的 CCR,在某种意义上,不是真正的 CCR,一个 46,XY,t(3;6)(p24;p21.2),inv(8)(p11;2q21.2) 男性患者的减数分裂分离,他的伴侣经历了三次早期流产后被转介。使用精子荧光原位杂交来筛选易位和倒位分离以及未涉及 CCR 的 13 条染色体的染色体间效应(ICE)。相互易位和着丝粒内倒位的错误分离率分别为 61.2%和 1.7%。ICE 分析显示,观察到的染色体非整倍体率在 0.1%至 0.8%之间,与对照值无显著差异。与对照精子(分别为 4.6%和 3.1%)相比,患者的累积 ICE 略有增加(P=0.049)。精子 DNA 碎片率与对照值有显著差异(5.0%;P=0.001)。在这个双重重排中,相互易位对着丝粒内倒位的减数分裂分离没有影响。无法得出关于着丝粒内倒位对易位影响的结论。

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