Results 71 to 80 of about 16,102 (215)

Long-term follow-up of patients with congenital diaphragmatic hernia

World Journal of Pediatric Surgery
Neonates with congenital diaphragmatic hernia encounter a number of surgical and medical morbidities that persist into adulthood. As mortality improves for this population, these survivors warrant specialized follow-up for their unique disease-specific ...
Terry L Buchmiller, Nicole Cimbak
doaj   +1 more source

Postnatal ultrasonography for evaluation of hernia sac of neonate with congenital diaphragmatic hernia

Radiology Case Reports, 2019
Congenital diaphragmatic hernia (CDH) is one of the most common major congenital anomalies. The presence of a hernia sac is associated with additional benefits in terms of improved neonatal survival.
Takahiro Hosokawa, MD, Yutaka Tanami, MD, Yumiko Sato, MD, Eiji Oguma, MD, Kanako Omata, MD, Hiroshi Kawashima, MD, Yoshitake Yamada, MD   +6 more
doaj   +1 more source

Right intrathoracic ectopic kidney and pulmonary sequestration associated with right sided congenital diaphragmatic hernia

Journal of Pediatric Surgery Case Reports, 2020
Intrathoracic ectopic kidney is an uncommon congenital anomaly, accounting for approximately 5% of all ectopic kidneys. An intrathoracic ectopic kidney and pulmonary sequestration associated with a congenital diaphragmatic hernia is a very rare condition.
Jinyoung Park
doaj   +1 more source

The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley, Gary F. Sholler, Janine Smith, Gillian M. Blue   +3 more
wiley   +1 more source

Fryns syndrome in children with congenital diaphragmatic hernia

, 2002
Fryns syndrome is characterized by multiple congenital anomalies including Congenital Diaphragmatic Hernia (CDH), and has a reported poor prognosis with a survival rate during the neonatal period of approximately 15%.
Jaksic, Tom, Congenital Diaphragmatic Hernia Study Group, Langham, Jr, Max R, Lally, Kevin P, Wilson, Jay M, Lally, Pamela A, Hirschl, Ronald B, Hardin, Jr, William D, Neville, Holly L   +8 more
core   +1 more source

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1821-1831, August 2026.
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair, Kevin Carratu, Natalie E. Rintoul, Holly L. Hedrick, William H. Peranteau, Catherine M. Avitabile, Kirsty McWalter, Paul Kruszka, Ian D. Krantz, K. Taylor Wild   +9 more
wiley   +1 more source

The management of congenital diaphragmatic hernia [PDF]

Canadian Anaesthetists’ Society Journal, 1966
On ne connait pas exactement la frequence de la hernie diaphragmatique congenitale, mais elle peut se presenter comme un cas d’extreme urgence chez le nouveau-ne. De 1959 a 1964, a 1’ “Hospital for Sick Children” de Toronto, on a opere d’urgence vingt-et-un nouveaux-nes durant les trente premieres heures de leur vie.
R E, Creighton, J S, Whalen, A W, Conn
openaire   +2 more sources

Newborn male presented with congenital diaphragmatic hernia and choledochal cyst: A case report

Journal of Pediatric Surgery Case Reports, 2015
Infants with congenital diaphragmatic hernia (CDH) have an increased incidence of associated malformations, ranging from 10% to 50% higher than the general population [1–5]. Choedochal cysts, congenital cystic dilations of the biliary tree, are anomalies
Daniel Krebs, Richard S. Herman, Christopher Blewett   +2 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Canine Congenital Diaphragmatic Hernia [PDF]

Journal of Veterinary Internal Medicine, 1988
Abstarct Congenital diaphragmatic hernia, affecting both sexes, was present in five of 27 puppies from three father-daughter matings. A purebred Golden Retriever was the common sire. The defect occurred in the left dorsolateral portion of the diaphragm, suggesting failure of closure of the left pleuroperitoneal canal during embryonic ...
B A, Valentine, B J, Cooper, A E, Dietze, D M, Noden   +3 more
openaire   +2 more sources