产前诊断胎儿先天性失氯性腹泻一例

doi:10.3877/cma.j.issn.1672-6448.2022.10.027

中华医学超声杂志（电子版） ›› 2022, Vol. 19 ›› Issue (10) : 1154 -1155. doi: 10.3877/cma.j.issn.1672-6448.2022.10.027

病例报告

产前诊断胎儿先天性失氯性腹泻一例

成晨¹, 赵胜¹, 陈欣林¹^,^†(

)

^1. 430070　武汉，湖北省妇幼保健院超声诊断科

收稿日期:2021-07-02 出版日期:2022-10-01
通信作者: 陈欣林
基金资助:
湖北省卫健委创新团队项目(WJ2018H0132)

Prenatal diagnosis of congenital chloride diarrhea: a case report

Chen Cheng¹, Sheng Zhao¹, Xinlin Chen¹()

Received:2021-07-02 Published:2022-10-01
Corresponding author: Xinlin Chen

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引用本文：

成晨, 赵胜, 陈欣林. 产前诊断胎儿先天性失氯性腹泻一例[J]. 中华医学超声杂志（电子版）, 2022, 19(10): 1154-1155.

Chen Cheng, Sheng Zhao, Xinlin Chen. Prenatal diagnosis of congenital chloride diarrhea: a case report[J]. Chinese Journal of Medical Ultrasound (Electronic Edition), 2022, 19(10): 1154-1155.

图1 先天性失氯性腹泻胎儿超声图像。图a为产前超声示羊水深度8.3 cm，内见密集的漂浮光点，类似果冻样回声；图b为产前超声示胎儿空肠和回肠广泛扩张，充满液体，肠壁回声强；图c为三维水晶成像见肠腔呈蜂巢状

1	Peter WC. 妇产科超声学 [M]. 常才, 戴晴, 谢晓燕, 译. 5版. 北京: 人民卫生出版社, 2010: 653-654.
2	Fuwa K, Hosono S, Nagano N, et al. Japanese neonate with congenital chloride diarrhea caused by SLC26A3 mutation [J]. Pediatr Int, 2015, 57(1): e11-e13.
3	Höglund P, Auranen M, Socha J, et al. Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait [J]. Am J Hum Genet, 1998, 63(3): 760-768.
4	Mustafa OM, Al-Aali WY. Honeycomb fetal abdomen: characteristic sign of congenital chloride diarrhea [J]. Ultrasound Obstet Gynecol, 2016, 48(6): 797-799.

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