Results 31 to 40 of about 1,114 (199)
Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome
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
Giant omphalocele: current perspectives
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,
Rogdo, Bjarte, Mack,Alexander Josef
+7 more sources
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
Introduction: Post-omphalocele ventral hernias pose significant challenges in pediatric surgery, often requiring multiple revision surgeries and carrying a high morbidity rate.
Mario Javier Peña García +8 more
doaj +1 more source
Evaluation of Omphalocele Treatment Using New Surgical Technique [PDF]
Introduction: The aim of this study was to evaluate a new technique for treatment of omphalocele using mesh fixation to skin with preserved omphalocele sac.
Askarpour, Shahnam +3 more
core +2 more sources
Conservative management of giant omphaloceles with hydrocolloid dressings
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
Prediction of postnatal outcome in foetuses at risk for chronic lung disease [PDF]
In this two-part thesis we assessed the value of prenatal ultrasound predictors for postnatal outcome in foetuses with a congenital anomaly associated with pulmonary hypoplasia and an increased risk of postnatal development of pulmonary hypertension and ...
Peters, Nina
core +5 more sources
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
Repair of giant omphalocele by component separation technique
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
Glucocorticoids for treating paediatric pulmonary hypertension: A novel use for a common medication [PDF]
Laboratory investigations have shown the role of inflammation in the pathogenesis of pulmonary hypertension and improvement after anti-inflammatory drugs.
Aggarwal, Manish, Grady, Ronald M
core +2 more sources

