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与单脐动脉相关的染色体异常。

Chromosomal abnormalities associated with a single umbilical artery.

作者信息

Khong T Y, George K

机构信息

Department of Pathology, Queen Victoria Hospital, Australia.

出版信息

Prenat Diagn. 1992 Nov;12(11):965-8. doi: 10.1002/pd.1970121118.

Abstract

A single umbilical artery was seen in 10 out of 117 cytogenetically abnormal pregnancies. The abnormal karyotypes found to be associated with a single umbilical artery were trisomy 18 (n = 5), monosomy X (n = 2), triploidy (n = 1), sex chromosome (47,XYY; n = 1) and translocation (46t(X,5)(q13p15);n = 1). With the exception of the translocation case, all cases with a single umbilical artery had anatomical defects which were detectable ultrasonographically. This suggests that a single umbilical artery alone is not an indication for prenatal fetal karyotyping.

摘要

在117例细胞遗传学异常妊娠中,有10例发现单脐动脉。发现与单脐动脉相关的异常核型有18三体(n = 5)、X单体(n = 2)、三倍体(n = 1)、性染色体(47,XYY;n = 1)和易位(46t(X,5)(q13p15);n = 1)。除易位病例外,所有单脐动脉病例均有超声可检测到的解剖学缺陷。这表明,仅单脐动脉本身并非产前胎儿核型分析的指征。

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