Results 41 to 50 of about 2,639 (198)

Concurrent Mesh Repair of a Morgagni and Umbilical Hernia during a Laparoscopic Sleeve Gastrectomy in a Morbidly Obese Individual [PDF]

open access: yesJournal of Krishna Institute of Medical Sciences University, 2016
Morgagni Hernia is a rare form of diaphragmatic hernia. It is mainly asymptomatic and often identified incidentally during surgery. Tension-free synthetic mesh repair is the preferred treatment modality.
N.R Kosai   +4 more
doaj  

Essential Anatomy for the Abdominal Wall Surgeon: Expert Consensus of Anatomical Concepts and Operative Steps for Posterior Component Separation

open access: yesWorld Journal of Surgery, Volume 49, Issue 12, Page 3390-3401, December 2025.
Abdominal wall surgery is emerging as a new subspecialty with reconstructive operations becoming increasingly complex. Central to any surgical subspecialty is comprehensive anatomical knowledge, which can be enhanced by cadaver dissection. An expert panel convened to develop a consensus framework highlighting key anatomical concepts and operative steps
Lawrence Nip   +12 more
wiley   +1 more source

Multidetector Computed Tomography Diagnosis of Gastric Volvulus through the Foramen of Morgagni

open access: yesJournal of the Belgian Society of Radiology, 2014
Morgagni hernia is considered to be the rarest form of all diaphragmatic hernias. It develops through a congenital defect in the retrosternal area.
Dr S. Lecouvet   +5 more
doaj   +1 more source

Laparoscopic assisted repair of a giant bilateral congenital Morgagni hernia associated with malrotation in an infant

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Introduction: Morgagni hernia is a rare congenital malformation accounting for less than 5% of all congenital diaphragmatic hernias. Patients may be asymptomatic or present with non-specific respiratory or gastrointestinal symptoms, which can delay the ...
Maira Lazzarini   +2 more
doaj   +1 more source

Nationwide Danish Register Based Study Showed a Stable Prevalence of Congenital Diaphragmatic Hernias From 1994 to 2021 but a Decrease in Syndromic Cases

open access: yesActa Paediatrica, Volume 114, Issue 12, Page 3252-3257, December 2025.
ABSTRACT Aim Congenital diaphragmatic hernia (CDH) is a severe malformation with high morbidity and mortality. This Danish study evaluated the birth prevalence, co‐occurring malformations, and temporal trends of CDH over nearly three decades. Methods Nationwide data from the Danish Biobank Register were used to identify liveborn infants diagnosed with ...
Ulrik Lausten‐Thomsen   +6 more
wiley   +1 more source

A rare case of Morgagni hernia associated with cor triatriatum

open access: yesJournal 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   +4 more
doaj   +1 more source

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

open access: yesClinical 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   +6 more
wiley   +1 more source

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

open access: yesAtti 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   +10 more
doaj   +1 more source

Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant

open access: yesAmerican 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   +7 more
wiley   +1 more source

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