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胎儿7号染色体部分单体性(q34→qter)和18号染色体部分三体性(q21→qter)的产前诊断。

Prenatal diagnosis of a fetus with partial monosomy 7(q34-->qter) and partial trisomy 18(q21-->qter).

作者信息

Pluchon E, Giovangrandi Y, Labbe F, Le Bris M J, Collet M, Brettes J P, Riviere D, Riviere M R

机构信息

Service d'Histologie Embryologie et Cytogénétique, Faculté de Médecine, Université de Bretagne Occidentale, Brest, France.

出版信息

Prenat Diagn. 1993 Oct;13(10):983-8. doi: 10.1002/pd.1970131013.

Abstract

Ultrasound examination of a 31-year-old woman at 27 weeks' gestation revealed fetal growth retardation, a bilateral cleft lip and palate, and the absence of median cerebral structures. Chromosome analysis after cordocentesis showed an abnormal karyotype with a structural abnormality of the long arm of chromosome 7: 46,XX,-7,+der(7),t(7;18) (q34;q21.3)mat. The pregnancy was terminated at week 29. The ultrasound findings were confirmed by post-mortem examination, which also revealed a semilobar holoprosencephaly.

摘要

一名31岁女性在妊娠27周时接受超声检查,结果显示胎儿生长受限、双侧唇腭裂以及大脑中部结构缺失。经皮脐血穿刺术后的染色体分析显示核型异常,存在7号染色体长臂的结构异常:46,XX,-7,+der(7),t(7;18) (q34;q21.3)mat。妊娠在第29周终止。尸检证实了超声检查结果,同时还发现了半侧叶型前脑无裂畸形。

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