Results 1 to 10 of about 14,204 (293)

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

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2014
ObjectiveWe describe a prenatal ultrasonography diagnosis of omphalocele and symbrachydactyly in a fetus and review the literature on prenatal diagnosis of 9p terminal chromosomal deletions.Case reportA 31-year-old woman (gravida 3, para 1) was referred ...
Chen, Chih-Ping   +6 more
core   +8 more sources

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

open access: yesBMC 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   +10 more
semanticscholar   +2 more sources

Additional Anomalies in Children with Gastroschisis and Omphalocele: A Retrospective Cohort Study

open access: yesChildren, 2023
Background: Congenital abdominal wall defects might be associated with other anomalies, such as atresia in gastroschisis and cardiac anomalies in omphalocele patients.
A. G. Pijpers   +7 more
semanticscholar   +3 more sources

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing

open access: yesAnnals of Medicine, 2021
Objectives The aim of this study is to share our experience in the prenatal diagnosis of omphalocele by karyotyping, chromosomal microarray analysis (CMA) and whole exome sequencing (WES). Methods In this retrospective study, 81 cases of omphalocele were
Xiaomei Shi   +5 more
semanticscholar   +3 more sources

Gastroschisis and omphalocele [PDF]

open access: yesWorld Journal of Surgery, 1993
It has been widely acknowledged that exomphalos and gastroschisis are two different clinical entities. Their etiology and pathogenesis, however, remain controversial.
Molenaar, J.C., Tibboel, D. (Dick)
core   +4 more sources

A Case Report of Patent Urachus With Perinatal Cardiac Abnormality. [PDF]

open access: yesClin Case Rep
ABSTRACT Patent urachus is a rare urachal anomaly. This case involves a newborn female with a cyst near the umbilicus and a small patent ductus arteriosus with left‐to‐right shunting. A low‐dose fluoroscopic cystogram revealed contrast entering a tubular structure extending from the bladder to the umbilicus, with evidence of leakage at the umbilical ...
Alzahrani HM.
europepmc   +2 more sources

OMPHALOCELE

open access: yesJOURNAL OBGIN EMAS, 2019
Tujuan: Melaporkan kasus omphaloceleMetode: Laporan kasusHasil: Kasus wanita berusia 24 tahun, dengan diagnosa G1P0A0H0 gravid aterm 37-38 minggu + omphalocele + IUGR. Pada pemeriksaan USG ditemukan biometri janin; BPD : 84 mm, FL : 67 mm, HL: 59 mm, AC : 305 mm, AFI : 8,8 cm, tampak massa menonjol dengan batas tegas pada dinding anterior ...
Muhammad Johar Nafis   +1 more
openaire   +3 more sources

Hepatic omphalocele in an adult [PDF]

open access: yesScandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery, 2004
The finding of an untreated omphalocele in adulthood is extremely rare. We report the case of a 29-year-old patient, who presented to us with a congenital defect of the abdominal wall and protrusion of underlying viscera.
BRONGO S   +4 more
core   +6 more sources

Neonate with omphalocele and dextrocardia: Anaesthetic goals and challenges

open access: diamondJournal 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.
VishalKrishna Pai   +3 more
openalex   +3 more sources

PIGO Gene Variants: New Insights Into Prenatal Diagnosis. [PDF]

open access: yesPrenat Diagn
Prenatal Diagnosis, Volume 45, Issue 8, Page 1058-1062, July 2025.
Zambiasi A   +6 more
europepmc   +2 more sources

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