Results 21 to 30 of about 46,426 (288)

Successful Repair of Congenital Morgagni Hernia and Ventricular Septal Defect via Median Sternotomy in a Patient with Down Syndrome, Anal Atresia, Pectus Carinatum and Congenital Hypothyroidism

open access: yesÇocuk Dergisi, 2023
Here we report a 5-month-old female patient with Down syndrome who was successfully operated on due to congenital Morgagni hernia and ventricular septal defect concomitantly via median sternotomy.
Buğra Harmandar, Hande İştar
doaj   +1 more source

Acquired Traumatic Diaphragmatic Hernia with Delayed Presentation in a Child

open access: yesSudan Journal of Medical Sciences, 2019
A congenital diaphragmatic hernia occurs because of embryologic defects in the diaphragm. Most patients with congenital diaphragmatic hernias present early rather than late in life, however, adults may present with a congenital hernia that was undetected
Nader Mutwakel Osman
doaj   +1 more source

Giant congenital diaphragmatic hernia in an adult [PDF]

open access: yes, 2014
Bochdalek hernia is the most common type of congenital diaphragmatic hernia. It appears frequently in infants but rarely in adults. We present the case of a 50-year-old female han patient with tremendous left-sided congenital posterolateral diaphragmatic
Guowei Che, Heng Du, Yubin Zhou
core   +1 more source

The case for early use of rapid whole-genome sequencing in management of critically ill infants: late diagnosis of Coffin-Siris syndrome in an infant with left congenital diaphragmatic hernia, congenital heart disease, and recurrent infections. [PDF]

open access: yes, 2018
Congenital diaphragmatic hernia (CDH) results from incomplete formation of the diaphragm leading to herniation of abdominal organs into the thoracic cavity. CDH is associated with pulmonary hypoplasia, congenital heart disease, and pulmonary hypertension.
Campo, Miguel Del   +7 more
core   +2 more sources

Our Incidence of Diaphragmatic Hernia Detected with MDCT in the Past Two Years [PDF]

open access: yesDüzce Tıp Fakültesi Dergisi, 2015
Aim: Diaphragmatic hernia develops as a result of extension of the intraabdominal organs to the thorax from a diaphragmatic defect which may be either a congenital fusion defect or subsequently formed defect(iatrojenic or traumatic).
Nesrin Atcı   +3 more
doaj  

Laparoscopic Management of Post Traumatic Diaphragmatic Hernia: Report of Two Cases and Review of Literature

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2018
Traumatic diaphragmatic rupture is a serious complication following abdominal-thoracic trauma and is often missed in acute phase due to the presence of concurrent injuries. It can present later as diaphragmatic hernia which carries high morbidity and
Mahendra Pratap Singh   +3 more
doaj   +1 more source

Concurrent congenital peritoneopericardial diaphragmatic hernia and bochdalek hernia in a neonate [PDF]

open access: yes, 2014
We present the first report of a neonate with, concurrent left sided Bochdalek hernia and peritoneopericardial diaphragmatic ...
Chad A Kort   +2 more
core   +1 more source

Single site laparoscopic repair of a Morgagni hernia in a pediatric patient

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Anterior diaphragmatic hernias through the foramen of Morgagni are rare accounting for about 3% of surgically treated diaphragmatic hernias. Current management of Morgagni type diaphragmatic hernias involves surgical intervention, which is traditionally ...
Amanda Muñoz   +3 more
doaj   +1 more source

Morphology of the Esophageal Hiatus: Is It Different in 3 Types of Hiatus Hernias? [PDF]

open access: yes, 2020
Background/aimsThe esophageal hiatus is formed by the right crus of the diaphragm in the majority of subjects. Contraction of the hiatus exerts a sphincter-like action on the lower esophageal sphincter (LES). The aim is to study the hiatal anatomy (using
Ghahremani, Gary   +5 more
core   +1 more source

A 22-Week-Old Fetus with Nager Syndrome and Congenital Diaphragmatic Hernia due to a Novel SF3B4 Mutation. [PDF]

open access: yes, 2014
Nager syndrome, or acrofacial dysostosis type 1 (AFD1), is a rare multiple malformation syndrome characterized by hypoplasia of first and second branchial arches derivatives and appendicular anomalies with variable involvement of the radial/axial ray. In
BOTTILLO, IRENE   +7 more
core   +1 more source

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