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Omphalocele with Dextrocardia - A Rare Association

Journal of Nepal Medical Association, 2009
Omphalocele is frequently associated with many other congenital malformations. In cardiac anomalies, association of omphalocele with dextrocardia has been rarely noticed before.
Vikal Chandra Shakya, C S Agrawal, N R Shrestha, K Dhungel, S Adhikary   +4 more
doaj   +1 more source

Management of giant omphalocele with intestinal perforation

Journal of Pediatric Surgery Case Reports, 2021
Case of a male infant delivered at 36 weeks of gestational age and found to have a giant omphalocele, later complicated by intestinal perforation. A giant omphalocele is an omphalocele with an opening greater than 5 cm in diameter and containing the ...
Ritah Chumdermpadetsuk, Sandra Kabagambe, Vincent Duron   +2 more
doaj   +1 more source

Syndromes and Disorders Associated with Omphalocele (III): Single Gene Disorders, Neural Tube Defects, Diaphragmatic Defects and Others

Taiwanese Journal of Obstetrics & Gynecology, 2007
Omphalocele can be associated with single gene disorders, neural tube defects, diaphragmatic defects, fetal valproate syndrome, and syndromes of unknown etiology.
Chih-Ping Chen
doaj   +1 more source

Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study

BMC Pregnancy and Childbirth, 2023
Background Patients with omphalocele, a midline abdominal wall defect at the umbilical cord base, have a low survival rate. However, the long-term outcomes of fetuses with prenatally diagnosed omphalocele have scarcely been studied.
Yanting Que, Meiying Cai, Fang Yang, Qingqiang Ji, Shuqi Zhang, Wenhui Huang, Yashi Gao, Bojing Zhou, Hailong Huang, Hua Cao, Na Lin   +10 more
doaj   +1 more source

Wandering spleen associated with omphalocele in a neonate: An unusual case with non-operative management

Journal of Pediatric Surgery Case Reports, 2017
Wandering spleen with a history of omphalocele is extremely rare. We encountered a male baby with wandering spleen associated with omphalocele. This case of wandering spleen in a neonate was diagnosed by ultrasound and computed tomography scans after ...
Daisuke Masui, Suguru Fukahori, Kimio Asagiri, Shinji Ishii, Nobuyuki Saikusa, Naoki Hashizume, Motomu Yoshida, Naruki Higasidate, Saki Sakamoto, Shiori Tsuruhisa, Yoshiaki Tanaka, Minoru Yagi   +11 more
doaj   +1 more source

Giant omphalocele treated with simple daily dressing changes

Journal of Pediatric Surgery Case Reports, 2022
Omphalocele, also called exomphalos, is an anterior abdominal wall midline defect of variable size involving the umbilical ring containing the herniated viscera into a sac made up of peritoneum, amnion and Wharton's jelly. Giant omphalocele is an extreme
Jayalaxmi shripati Aihole
doaj   +1 more source

Neonate with omphalocele and dextrocardia: Anaesthetic goals and challenges

Journal of Medical Sciences, 2016
Omphalocele and gastroschisis are the two common congenital malformations of the anterior abdominal wall. Omphalocele can be associated with other congenital anomalies such as cardiac anomalies.
Vishal Krishna Pai, Mridul Dhar, Anil Prasad Singh, Atchya Arun Kumar   +3 more
doaj   +1 more source

Giant omphalocele closure utilizing botulinum toxin

Journal of Pediatric Surgery Case Reports, 2020
An omphalocele is a rare congenital abdominal wall defect of the umbilical ring. A giant omphalocele is typically defined as 5 cm or larger. Here we present a case of utilizing botulinum toxin to aid in closure of a giant omphalocele.
Jessica L. Rauh, Leah M. Sieren
doaj   +1 more source

Chromosomal Abnormalities Associated With Omphalocele

Taiwanese Journal of Obstetrics & Gynecology, 2007
Fetuses with omphalocele have an increased risk for chromosomal abnormalities. The risk varies with maternal age, gestational age at diagnosis, association with umbilical cord cysts, complexity of associated anomalies, and the contents of omphalocele ...
Chih-Ping Chen
doaj   +1 more source

Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies

Taiwanese Journal of Obstetrics & Gynecology, 2014
Objective: We describe a prenatal ultrasonography diagnosis of omphalocele and symbrachydactyly in a fetus and review the literature on prenatal diagnosis of 9p terminal chromosomal deletions.
Wen-Chien Hou, Chih-Ping Chen, Kwei-Shuai Hwang, Ying-Chieh Chen, Yu-Ju Lai, Chau-Yang Tien, Her-Young Su   +6 more
doaj   +1 more source