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孕早期自然流产样本中染色体异常的发生率及分布情况

Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions.

作者信息

Guerneri S, Bettio D, Simoni G, Brambati B, Lanzani A, Fraccaro M

机构信息

I Clinica Ostetrica et Ginecologica, Università di Milano, Italy.

出版信息

Hum Reprod. 1987 Nov;2(8):735-9. doi: 10.1093/oxfordjournals.humrep.a136623.

Abstract

Cytogenetic analysis was performed directly on villus material from 202 samples obtained at the evacuation of the uterine cavity in cases of retained abortion in the first trimester, identified as such by ultrasound examination. A precise delineation of the karyotype was obtained in 94% of the cases, while the efficiency of karyotype analysis in samples of spontaneous abortion was not higher than 50%. An abnormal chromosome constitution was found in 145 fetuses (76.7%) of which 117, including mosaics, were aneuploid (70%), 16 polyploid (8.5%) and 12 had structural abnormalities (6.3%). The relative proportion of chromosome abnormalities in this material is higher than that found in spontaneous abortion for trisomies and double trisomies, but lower for 45,X and polyploidy. The method was found to be efficient in obtaining fetal karyotypes also in those cases in which the villous material was scarce (1 mg), and thus it seems appropriate for routine cytogenetic studies in the first trimester abortions.

摘要

对孕早期稽留流产患者经超声检查确诊后行清宫术获取的202份绒毛组织直接进行细胞遗传学分析。94%的病例获得了精确的核型,而自然流产样本的核型分析效率不高于50%。在145例胎儿(76.7%)中发现染色体构成异常,其中117例(包括嵌合体)为非整倍体(70%),16例为多倍体(8.5%),12例有结构异常(6.3%)。该材料中染色体异常的相对比例在三体和双三体方面高于自然流产中的比例,但在45,X和多倍体方面低于自然流产。该方法在绒毛组织稀少(1mg)的病例中也能有效地获得胎儿核型,因此似乎适用于孕早期流产的常规细胞遗传学研究。

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