Results 81 to 90 of about 1,162 (183)

Untreated patient of Pentalogy of Cantrell surviving into the sixth decade: A unique case report

IHJ Cardiovascular Case Reports, 2018
Pentalogy of Cantrell is a rare syndrome consisting of a constellation of congenital anomalies including omphalocoele, lower sternal defect, sdiaphragmatic defect, diaphragmatic pericardial defect and congenital heart disease.
Neha Nischal, Sakshi Arya, Sunil Kumar Puri, Vijay Kumar Trehan   +3 more
doaj   +1 more source

Mortality in neonates with giant omphalocele subjected to a surgical technique in Barranquilla, Colombia from 1994 to 2019

Scientific Reports, 2021
No studies of the efficacy and safety of surgical techniques for the primary closure of giant omphalocele have been performed in Colombia. To determine the mortality rate and factors associated with mortality in neonates with giant omphalocele subjected ...
Alexander Barrios-Sanjuanelo, Cristóbal Abelló-Munarriz, Jaiberth Antonio Cardona-Arias   +2 more
doaj   +1 more source

Clinical and Surgical Perspectives on Isolated Thoracic Ectopia Cordis: A Rare Case Report

Case Reports in Pediatrics, Volume 2025, Issue 1, 2025.
Ectopia cordis is an exceptionally uncommon congenital condition where the heart develops outside its normal position due to incomplete closure of the ventral chest wall during embryogenesis. The anomaly may occur in isolation or with other structural defects, often resulting in a poor prognosis despite advancements in medical and surgical care.
Syed Mohsin Raza Bukhari, Hassan Mehdi, Maham Zaman, Nithya Venkatesh, Ammar Abbas, Ishrat Fatima, Aqsa Farooq, Hassaan Raza, Mohsin Raza, Nikhat Kaura   +9 more
wiley   +1 more source

Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997–2019

American Journal of Medical Genetics Part A, Volume 194, Issue 8, August 2024.
Abstract Craniofacial microsomia (CFM) primarily includes specific head and neck anomalies that co‐occur more frequently than expected. The anomalies are usually asymmetric and affect craniofacial features; however, there are frequently additional anomalies of variable severity. Published prenatal findings for CFM are limited. This study contributes 11
Mary Ann Thomas, Tanya Bedard, Susan Crawford, R. Brian Lowry   +3 more
wiley   +1 more source

Prenatal Diagnosis of Pentalogy of Cantrell

Journal of Diagnostic Medical Sonography, 2007
Pentalogy of Cantrell is a rarely seen syndrome that, in full form, includes a midline supraumbilical abdominal defect, defect of the lower sternum, deficiency of the diaphragmatic pericardium, deficiency of the anterior diaphragm, and congenital cardiac anomalies. Cases not fulfilling these criteria but including various combinations of them, provided
Tinar, S., Oztekin, D., Yildiz, I., Adibelli, Z., Oztekin, O., Öztekin, Özer.   +5 more
openaire   +3 more sources

Eliminating first trimester combined testing: Consequences for early detection of significant fetal anomalies

Prenatal Diagnosis, Volume 44, Issue 5, Page 544-554, May 2024.
Abstract Objective To determine whether implementation of cell‐free DNA (cfDNA) testing for aneuploidy as a first‐tier test and subsequent abolition of first trimester combined testing (FCT) affected the first trimester detection (<14 weeks) of certain fetal anomalies. Methods We performed a geographical cohort study in two Fetal Medicine Units between
M. A. Lugthart, H. Heinrich, I. Ertugrul, E. N. Nsiah‐Asare, K. van de Kamp, I. H. Linskens, M. C. van Maarle, E. van Leeuwen, E. Pajkrt   +8 more
wiley   +1 more source

Primary versus Staged Closure of Exomphalos Major: Cardiac Anomalies Do Not Affect Outcome [PDF]

, 2018
Aim: The objective of the study is to describe management of exomphalos major and investigate the effect of congenital cardiac anomalies. / Methods: A single-center retrospective review (with audit approval) was performed of neonates with exomphalos ...
Cross, KMK, Curry, JI, De Coppi, P, Eaton, SJ, Kiely, EM, Pierro, A, Rees, CM, Yates, RW   +7 more
core  

Morgagni hernia repair in children over two decades: Institutional experience, systematic review, and meta-analysis of 296 patients [PDF]

, 2018
BACKGROUND/PURPOSE: Morgagni diaphragmatic hernia (MH) is rare. We report our experience based on routine patch use in MH repair to curb recurrence. A systematic review and meta-analysis were performed to study the recurrence and complications associated
Banerjee, D, Blackburn, SC, Cross, KM, Curry, JI, De Coppi, P, Eaton, S, Giuliani, S, GOSH team, Rees, CM, Tan, Y-W   +9 more
core   +1 more source

A Case Report of Thoracic Ectopia Cordis in a Hospital in Zanjan, Iran

Case Reports in Pediatrics, Volume 2024, Issue 1, 2024.
Background and Aim. Ectopia cordis is a rare congenital anomaly characterized by the heart being located partially or completely outside of the thoracic cavity. Thoracic ectopia cordis is an even rarer form of this anomaly, with only a few reported cases in the literature. The aim of this study was to present the clinical and radiological findings of a
Mehdi Hosseini, Hassan Zamani, Shadi Moghimi, Aref Nekoufar, Sathyaprasad Burjonrappa   +4 more
wiley   +1 more source

First Trimester Diagnosis of Cantrell Pentalogy: A Case Report

Gynecology Obstetrics & Reproductive Medicine, 2015
Pentalogy of Cantrell is a rare syndrome with a deficiency of anterior diaphragm, a midline supraumbilical abdominal wall defect, a defect in the diaphragmatic pericardium, various congenital intracardiac abnormalities and a defect of the lower sternum.
Emel Ebru Özçimen, Ali Sami Gürbüz, Necati Özçimen   +2 more
doaj