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胎儿腹壁缺陷:一家三级医疗中心的六年经验

Fetal abdominal wall defects: six years experience at a tertiary center.

作者信息

Ekin A, Gezer C, Taner C E, Ozeren M, Avci M E, Ciftci S, Dogan A, Gezer N S

出版信息

Clin Exp Obstet Gynecol. 2015;42(3):327-30.

PMID:26152003
Abstract

The authors' aim was to detect the associated anomalies and their effect on the management of the fetuses with omphalocele and gastroschisis. Between the period of 2007-2013, the data of fetuses with abdominal wall defects were analyzed. Chromosomal abnormalities and associated morphologic anomalies diagnosed by ultrasonography and autopsy were evaluated. Of the. 61 fetuses, ten (20.4%) omphalocele cases and nine (75%) gastroschisis cases were isolated. Chromosomal abnormalities were found in seven fetuses with omphalocele cases. All fetuses with abnormal karyotypes had multiple additional anomalies. Termination rate was 65.3% for omphalocele group versus none in the gastroschisis group. To give better counseling about the prognosis and outcome of the fetuses with abdominal wall defects, detection of additional anomalies as well as type of the defect are essential tools even if the karyotype is normal.

摘要

作者的目的是检测合并的异常情况及其对腹裂和脐膨出胎儿治疗的影响。在2007年至2013年期间,对腹壁缺陷胎儿的数据进行了分析。评估了通过超声检查和尸检诊断出的染色体异常和相关形态学异常。在61例胎儿中,10例(20.4%)脐膨出病例和9例(75%)腹裂病例为孤立性病例。在脐膨出病例的7例胎儿中发现了染色体异常。所有核型异常的胎儿都有多种其他异常。脐膨出组的终止妊娠率为65.3%,而腹裂组则无终止妊娠情况。为了更好地为腹壁缺陷胎儿的预后和结局提供咨询,即使核型正常,检测其他异常以及缺陷类型也是至关重要的工具。

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引用本文的文献

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Omphalocele prevalence and co-occurring malformations: a nationwide register-based study of Danish live births in 1997-2021.脐膨出的患病率和伴发畸形:1997-2021 年丹麦活产儿的全国注册研究。
Pediatr Surg Int. 2024 Nov 22;41(1):1. doi: 10.1007/s00383-024-05897-5.
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A clinical-pathogenetic approach on associated anomalies and chromosomal defects supports novel candidate critical regions and genes for gastroschisis.一种针对相关异常和染色体缺陷的临床-发病机制方法支持腹裂新的候选关键区域和基因。
Pediatr Surg Int. 2018 Sep;34(9):931-943. doi: 10.1007/s00383-018-4331-4. Epub 2018 Aug 9.