Results 31 to 40 of about 2,899 (173)

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

Recurrent late complications following congenital diaphragmatic hernia repair with prosthetic patches: a case series

open access: yesJournal of Medical Case Reports, 2009
Introduction Many different prosthetic materials have been used for repair of large posterolateral congenital diaphragmatic hernias, which cannot be primarily repaired. Almost 50% of patch repaired diaphragmatic hernias will recur.
Bekdash Basil   +2 more
doaj   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim   +2 more
wiley   +1 more source

Current Nationwide Landscape of Cardiac Surgery for Children With Trisomy 18 in Japan

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Despite the increasing number of retrospective cohorts describing successful cardiac surgery for children with trisomy 18, no consensus has been reached among healthcare providers regarding cardiac surgery in Japan. This study provided a benchmark to facilitate consensus building by assessing a nationwide surgical database in Japan. A total of
Shintaro Nemoto   +5 more
wiley   +1 more source

Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato   +2 more
wiley   +1 more source

Laparoscopic repair of congenital pleuroperitoneal hernia using a polypropylene mesh in a dog

open access: yesArquivo Brasileiro de Medicina Veterinária e Zootecnia, 2015
Pleuroperitoneal hernias are the most uncommon type of diaphragmatic hernias in dogs and cats. The treatment of choice is surgery and may involve the use of prosthetic implant through celiotomy.
H.F. Hartmann   +8 more
doaj   +1 more source

Klippel‐Trénaunay‐Weber Syndrome: Prenatal Diagnosis and Review of the Literature

open access: yesJournal of Clinical Ultrasound, Volume 53, Issue 3, Page 535-546, March/April 2025.
This meta‐analysis demonstrates the high diagnostic accuracy of SZ‐CEUS for differentiating between malignant and benign focal liver lesions, as well as for HCC from non‐HCC lesions. The study shows better performance for smaller lesions and those with a higher proportion of malignancy.
Giuliana Orlandi   +13 more
wiley   +1 more source

Ileus and Late-onset Traumatic Diaphragmatic Hernia Presenting with Vomiting and Dyspnea: A Case Report

open access: yesJournal of Pediatric Emergency and Intensive Care Medicine, 2022
Diaphragmatic hernia is defined as the passage of abdominal organs through the diaphragmatic muscle and can be congenital or acquired. Motor vehicle accidents are the most common cause of acquired hernias in children.
Pelin Elibol   +7 more
doaj   +1 more source

Congenital diaphragmatic hernia

open access: yes, 2021
Congenital diaphragmatic hernia occurs in 1–5/10,000 live births. It is characterized by a defect in the separation of the thoracic cavity from the abdominal cavity due to incomplete development of the diaphragm. It follows the herniation of abdominal viscera at the thoracic level with hypoplasia of the lung ipsilateral to the hernia.
Boonthai, Ampaipan, Losty, Paul D
openaire   +3 more sources

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