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人类自然流产中染色体的Q带分析

Q-banding of chromosomes in human spontaneous abortions.

作者信息

Carr D H, Gedeon M M

出版信息

Can J Genet Cytol. 1978 Sep;20(3):415-25. doi: 10.1139/g78-048.

Abstract

Chromosome studies of 242 spontaneous abortions were carried out by Q-banding technique. The abortuses were selected for study because they were phenotypically abnormal, had not progressed beyond 12 weeks development or were from women with repeated abortions. Chromosome anomalies were found in 126 (52%) of the abortuses. Of these, 71 (56%) were trisomies. Trisomies were found for all the autosomes except Nos. 1, 3, 5, 11, 17 and 18. Triploidy was the second commonest anomaly in this series, making up 26 (21%) of the total anomalies. About 70% of these had an XXY sex chromosome complement. Only 16 (13%) of the abortuses had X monosomy, a lower frequency than would be expected in an unselected study. Tetraploidy was found in 8 abortuses and the 5 remaining specimens had various anomalies. These included 3 translocations, a trisomy 21,X monosomy and a ring chromosome 13. Except for the greater frequency of XXY than XXX sex chromosomes in the triploids, there was no evidence of a distortion of the sex ratio, either among the trisomic or among the chromosomally normal abortuses.

摘要

采用Q带技术对242例自然流产胎儿进行了染色体研究。选择这些流产胎儿进行研究是因为它们在表型上异常、发育未超过12周或来自有反复流产史的妇女。在126例(52%)流产胎儿中发现了染色体异常。其中,71例(56%)为三体性。除1、3、5、11、17和18号常染色体外,所有常染色体均发现了三体性。三倍体是该系列中第二常见的异常,占总异常的26例(21%)。其中约70%具有XXY性染色体组成。只有16例(13%)流产胎儿为X单体性,其频率低于非选择性研究中的预期频率。在8例流产胎儿中发现了四倍体,其余5个标本有各种异常。这些异常包括3例易位、1例21三体、X单体性和1例13号环状染色体。除三倍体中XXY性染色体比XXX性染色体频率更高外,在三体性流产胎儿或染色体正常的流产胎儿中均没有证据表明性别比存在偏差。

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