Sac-Type Congenital Diaphragmatic Hernia: A Case Report of Two Siblings

Congenital diaphragmatic hernia (CDH), a herniation of the abdominal contents through a defect or hypoplasia of the diaphragm, is a relatively common, severe congenital anomaly. Here we present the first case of two siblings with possibly isolated sac-type CDH and with a suspected genetic etiology....

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Bibliographic Details
Main Authors: Chisato Kodera, Takashi Ohba, Tomomi Hashimoto, Munekage Yamaguchi, Hidetaka Yoshimatsu, Hidetaka Katabuchi
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2018/3270526
Description
Summary:Congenital diaphragmatic hernia (CDH), a herniation of the abdominal contents through a defect or hypoplasia of the diaphragm, is a relatively common, severe congenital anomaly. Here we present the first case of two siblings with possibly isolated sac-type CDH and with a suspected genetic etiology. Although sibling recurrence of isolated CDH is rare, the incidence is higher than in the general population. Additionally, the second child had a more severe respiratory disorder than the first child. It is to be noted that siblings of children having isolated CDH are at risk for CDH, and prenatal evaluation should be considered individually.
ISSN:2090-6684
2090-6692