Results 71 to 80 of about 143,923 (179)

Cardiac Tamponade During Congenital Diaphragmatic Hernia Repair in an Infant: A Case Report and Literature Review

Clinical Case Reports, Volume 13, Issue 11, November 2025.
Schematic depiction of congenital diaphragmatic hernia with abdominal organs displaced into the chest, accompanied by visual elements illustrating the key complications observed in this case: cardiac tamponade and pleural effusion. Created in BioRender. Davoodi Karsalari, P. (2025) https://BioRender.com/n8wws0e.
Pershia Davoodi Karsalari, Aylar Mohammadi, Noosha Samieefar, Gholamreza Ebrahimisaraj, Mehdi Sarafi, Nastaran Sadat Mahdavi, Parinaz Alizadeh   +6 more
wiley   +1 more source

Hérnia de Morgagni simulando lipoma torácico

Revista do Colégio Brasileiro de Cirurgiões
The Morgagni hernia is the rarest kind of diaphragmatic hernia , occurring in 3% of all cases. It consists of the protrusion of the abdominal content into the thoracic cavity including omentum and transverse colon, among others.
Elias Amorim, Jairo de Sousa Pacheco
doaj   +1 more source

A rare case of Morgagni hernia associated with cor triatriatum

Journal of Pediatric Surgery Case Reports, 2015
The Morgagni hernia is a rare congenital disorder that is often associated with other anomalies such as congenital heart disease. We present here a case of Morgagni hernia with concomitant cor triatriatum, both of which were repaired in one operation via
Xicheng Deng, Pingbo Liu, Liwen Yi, Jinghua Wang, Peng Huang   +4 more
doaj   +1 more source

Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Loeys‐Dietz syndrome (LDS) is a heritable connective tissue disorder with variable expressivity. It is a multisystemic condition mainly characterized by a propensity for arterial aneurysms and dissections, skeletal manifestations, hypertelorism, bifid uvula, craniosynostosis, and cutaneous features.
Noémie Villeneuve‐Cloutier, Christie A Boswell‐Patterson, Lucas Bronicki, Krista M. Vincent, Kalin Wilk, Andrea C. Yu, Gail E. Graham, Julie Richer   +7 more
wiley   +1 more source

Impact of fetal treatments for congenital diaphragmatic hernia on lung development

The Anatomical Record, Volume 308, Issue 4, Page 1066-1081, April 2025.
Abstract The extent of lung hypoplasia impacts the survival and severity of morbidities associated with congenital diaphragmatic hernia (CDH). The alveoli of CDH infants and in experimental models of CDH have thickened septa with fewer type II pneumocytes and capillaries. Fetal treatments of CDH‐risk preterm birth.
Mar Janna Dahl, Anna Lavizzari, Jonathan W. Davis, Peter B. Noble, Raffaele Dellacà, J. Jane Pillow   +5 more
wiley   +1 more source

UEG Week 2023 Oral Presentations

, 2023
United European Gastroenterology Journal, Volume 11, Issue S8, Page 9-200, October 2023.
wiley   +1 more source

Bilateral Morgagni Hernia: A Unique Presentation of a Rare Pathology

Case Reports in Radiology, 2016
Morgagni hernia is an unusual congenital herniation of abdominal content through the triangular parasternal gaps of the anterior diaphragm. They are commonly asymptomatic and right-sided.
Michael Leshen, Randy Richardson
doaj   +1 more source

Right heart tamponade and intermittent cyanosis due to Morgagni diaphragmatic hernia in a neonate

Journal of Pediatric Surgery Case Reports, 2020
Congenital Morgagni hernia (CMH) is a rare congenital anomaly is typically diagnosed in childhood and on occasions in adults during work up of unexplained respiratory infections or gastrointestinal symptoms.
Umesh Dyamenahalli, Paula Williams, Thomas K. Lee   +2 more
doaj   +1 more source

Robotic approach to Morgagni-Larrey hernia in pediatric surgery: a case report

Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, 2022
Morgagni-Larrey hernias represent a subgroup of Congenital diaphragmatic hernias (CDHs), involving the anterior part of the muscle. They are complex developmental defects often representing a diagnostic and treatment challenge for both pediatricians and ...
Giada Loria, Flora Maria Peri, Donatella Di Fabrizio, Grazia Giulia Pantè, Serena Scalise, Pietro Antonuccio, Pietro Impellizzeri, Ignazio Salamone, Claudio Romano, Girolamo Mattioli, Carmelo Romeo   +10 more
doaj   +1 more source

Mesenchymal retinoic acid signaling is required for normal diaphragm development in mice

The FASEB Journal, Volume 39, Issue 3, 15 February 2025.
Single‐cell sequencing analysis of mouse pleuroperitoneal folds shows that genes associated with congenital diaphragmatic hernia and retinoic acid signaling are primarily expressed in the non‐muscular mesenchyme of the developing diaphragm. Blocking mesenchymal retinoic acid signaling in the developing diaphragm of Prrx1Cre:RARdn mice causes congenital
Juan F. Garcia Rivas, Nicole H. M. Applin, Jaida F. P. Albrechtsen, Adibehalsadat Ghazanfari, Michael Doschak, Robin D. Clugston   +5 more
wiley   +1 more source