Results 41 to 50 of about 358,897 (181)

Repair of ruptured omphalocele sac in the neonatal period and beyond

open access: yesJournal of Indian Association of Pediatric Surgeons, 2020
Conservative management of giant omphalocele in the neonate period is a known strategy to allow tissue growth aiding in anatomical closure. However, rupture of the covering sac is considered an absolute contraindication for continuing conservative ...
Nidhi Sugandhi   +3 more
doaj   +1 more source

Vaginal Delivery in Cases of Prenatally Diagnosed Omphalocele: Feasibility and Outcomes. [PDF]

open access: yesPrenat Diagn
ABSTRACT Objective This study aimed to assess outcomes of fetuses with prenatally detected omphalocele and the frequency of successful vaginal delivery in pregnancies with suspected non‐lethal omphalocele and intended active neonatal management and its impact on neonatal outcome.
Heinrich H   +5 more
europepmc   +2 more sources

Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome

open access: yesPrenatal Diagnosis, Volume 43, Issue 2, Page 183-191, February 2023., 2023
Abstract Objective Omphalocele is known to be associated with genetic anomalies like trisomy 13, 18 and Beckwith–Wiedemann syndrome, but not with Turner syndrome (TS). Our aim was to assess the incidence of omphalocele in fetuses with TS, the phenotype of this association with other anomalies, their karyotype, and the fetal outcomes.
Ivonne Bedei   +25 more
wiley   +1 more source

Vacuum-assisted staged omphalocele reduction: A preliminary report

open access: yesFrontiers in Pediatrics, 2022
IntroductionOmphalocele represents a rare congenital abdominal wall defect. In giant omphalocele, due to the viscero-abdominal disproportion, gradual reintegration of eviscerated organs is often associated with medical challenges.
Matthias Nissen   +5 more
doaj   +1 more source

Association of omphalocele with a patent urachus presenting as a large umbilical cystic mass in a newborn

open access: yesClinical Case Reports, Volume 9, Issue 8, August 2021., 2021
Simultaneous presentation of omphalocele, patent urachus, and umbilical cyst is very rare. There is wide range of differential diagnosis for umbilical cyst. Accurate assessment of umbilical cysts is important to evaluate other abnormalities. Abstract Simultaneous presentation of omphalocele, patent urachus, and umbilical cyst is very rare.
Roya Farhadi, Seyed Abdollah Mousavi
wiley   +1 more source

Giant omphalocele: current perspectives

open access: yesResearch and Reports in Neonatology, 2016
Alexander Josef Mack,1 Bjarte Rogdo2 1Department of Pediatric Surgery, 2Pediatric and Neonatal Intensive Care Unit, Children’s Hospital of Eastern Switzerland, St Gallen, Switzerland Abstract: Giant omphalocele (GO) is a congenital ventral abdominal wall defect characterized by a large opening with herniated abdominal organs, including liver,
Mack,Alexander Josef, Rogdo,Bjarte
  +7 more sources

Conservative management of giant omphaloceles with hydrocolloid dressings

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Omphalocele is a life-threatening abdominal wall defect without a treatment consensus due to its increased risk of complications. Discrepancies exist between a prompt or a delayed closure.
Estefania Roldan-Vasquez, MD   +3 more
doaj   +1 more source

Ruptured Giant Omphalocele. A Case Report

open access: yesMedisur, 2013
Omphalocele is one of the abdominal wall defects. It can be associated with other malformations including imperforate anus, agenesis of the colon, bladder exstrophy and cardiovascular disease, frequently leading to non-viable fetuses.
Víctor Manuel González Valdez   +2 more
doaj   +1 more source

Repair of giant omphalocele by component separation technique

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Giant omphalocele management has always been a challenge because of the large fascial defect and the associated anomalies. We managed successfully a neonate with giant omphalocele and no associated anomalies by delayed repair constituting escharotic ...
Mutua Irene, Swaleh Shahbal
doaj   +1 more source

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
doaj   +1 more source

Home - About - Disclaimer - Privacy