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体外受精后人类未受精卵母细胞和未受精卵裂合子中染色体异常的发生率。

The frequency of chromosome anomalies in human unfertilized oocytes and uncleaved zygotes after insemination in vitro.

作者信息

Papadopoulos G, Randall J, Templeton A A

机构信息

Department of Obstetrics and Gynaecology, University of Aberdeen, Foresterhill, UK.

出版信息

Hum Reprod. 1989 Jul;4(5):568-73. doi: 10.1093/oxfordjournals.humrep.a136945.

DOI:10.1093/oxfordjournals.humrep.a136945
PMID:2794016
Abstract

Data on first trimester human abortions have shown chromosome aberrations in approximately 50% of the cases, most of which were trisomies. More than 80% of these trisomies have been attributed to an error in the oocyte. In this study we investigated the frequency of chromosome anomalies in 44 human unfertilized oocytes and 13 uncleaved zygotes after insemination in vitro. The oocytes were aspirated from preovulatory follicles in parous volunteer donors and patients participating in an embryo replacement programme. Thirty cases could be analysed, 18 of which (60%) carried a chromosome abnormality. There were two hyperhaploidies (6.7%), four hypohaploidies (13.3%), three polyploidies (10%), six with structural aberrations (20%) and five diploidies (16.7%). The incidence of these abnormalities, except for the structural anomalies, was similar to that reported previously. The higher frequency of structural aberrations in the present study may be related to delayed cytogenetic analysis for up to 48 h after insemination.

摘要

关于孕早期人工流产的数据显示,约50%的病例存在染色体畸变,其中大多数为三体性。这些三体性中超过80%归因于卵母细胞的错误。在本研究中,我们调查了44个人类未受精卵母细胞和13个体外受精后未分裂的合子中染色体异常的频率。卵母细胞是从经产妇志愿者供体和参与胚胎置换计划的患者的排卵前卵泡中抽吸的。30个病例可供分析,其中18个(60%)存在染色体异常。有2个超单倍体(6.7%)、4个亚单倍体(13.3%)、3个多倍体(10%)、6个有结构畸变(20%)和5个二倍体(16.7%)。除结构异常外,这些异常的发生率与先前报道的相似。本研究中结构畸变的较高频率可能与受精后长达48小时的细胞遗传学分析延迟有关。

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The frequency of chromosome anomalies in human unfertilized oocytes and uncleaved zygotes after insemination in vitro.体外受精后人类未受精卵母细胞和未受精卵裂合子中染色体异常的发生率。
Hum Reprod. 1989 Jul;4(5):568-73. doi: 10.1093/oxfordjournals.humrep.a136945.
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引用本文的文献

1
Human oocyte chromosome analysis: complicated cases and major pitfalls.人类卵母细胞染色体分析:复杂病例与主要陷阱
J Genet. 2008 Aug;87(2):147-53. doi: 10.1007/s12041-008-0022-6.
2
Chromosomal analysis of unfertilized human oocytes prepared by a gradual fixation-air drying method.采用逐步固定-空气干燥法制备的未受精人类卵母细胞的染色体分析。
Hum Genet. 1993 Jan;90(5):533-41. doi: 10.1007/BF00217454.
3
The preimplantation genetic diagnosis of genetic diseases.
J In Vitro Fert Embryo Transf. 1990 Feb;7(1):1-5. doi: 10.1007/BF01133875.
4
Chromosomal analysis of unfertilized oocytes and morphologically abnormal preimplantation embryos from an in vitro fertilization program.对来自体外受精项目的未受精卵母细胞和形态异常的植入前胚胎进行染色体分析。
J In Vitro Fert Embryo Transf. 1990 Dec;7(6):341-6. doi: 10.1007/BF01130587.
5
Predivision in human oocytes at meiosis I: a mechanism for trisomy formation in man.人类卵母细胞减数分裂I期的提前分裂:人类三体形成的一种机制。
Hum Genet. 1991 Feb;86(4):383-7. doi: 10.1007/BF00201839.
6
Frequency and distribution of aneuploidy in human female gametes.人类雌性配子中非整倍体的频率与分布
Hum Genet. 1991 Jan;86(3):283-8. doi: 10.1007/BF00202410.
7
Cytogenetics of human oocytes, zygotes, and embryos after in vitro fertilization.
Hum Genet. 1992 Feb;88(4):367-75. doi: 10.1007/BF00215667.
8
Factors associated with premature chromosome condensation (PCC) following in vitro fertilization.体外受精后与早熟染色体凝集(PCC)相关的因素。
J Assist Reprod Genet. 1992 Feb;9(1):61-7. doi: 10.1007/BF01204117.