Results 31 to 40 of about 8,597 (234)

Fetal heterotaxy with tricuspid atresia, pulmonary atresia, and isomerism of the right atrial appendages at 22 weeks. [PDF]

open access: yes, 2013
We report the accurate prenatal diagnosis at 22 weeks gestation of right atrial isomerism in association with tricuspid atresia. Several distinctive sonographic features of isomerism of the right atrial appendages were present in this fetus: complex ...
Richardson, Randy R   +3 more
core   +2 more sources

Association of Intestinal Malrotation and Bochdalek Hernia in an Adult: a Case Report [PDF]

open access: yes, 2014
Background Late presentations of congenital diaphragmatic hernia are rare and differ from the classic neonatal presentation. The association with other congenital malformations in children, mainly intestinal malrotation, is well documented.
Fradique, AC   +5 more
core   +1 more source

Spectrum of Clinical and Radiological Presentation of Midgut Malrotation in Children and Adolescents: Case Series

open access: yesJournal of Gastrointestinal and Abdominal Radiology, 2022
Midgut malrotation is usually present in the early neonatal period with intestinal obstruction and bilious vomiting. However, sometimes it may present later in childhood and adolescence with atypical features and then may remain undiagnosed for long ...
Saurya Saurya   +3 more
doaj   +1 more source

A Rare Cause of Acute Abdomen in Adults: Intestinal Malrotation

open access: yesHaseki Tıp Bülteni, 2017
Intestinal malrotation is a congenital anomaly of the midgut. The incidence of intestinal malrotation is 1 in 500 live births. It is rarely seen in adults.
Mürşit Dinçer   +2 more
doaj   +1 more source

The route and timing of hydrogen sulfide therapy critically impacts intestinal recovery following ischemia and reperfusion injury [PDF]

open access: yes, 2018
PURPOSE: Hydrogen sulfide (H2S) has many beneficial properties and may serve as a novel treatment in patients suffering from intestinal ischemia-reperfusion injury (I/R).
Drucker, Natalie A.   +4 more
core   +1 more source

Malrotation of Intestine with Carcinoma Colon in Adult

open access: yesJournal of Nepal Medical Association, 2014
Malrotation of gut is a congenital anomaly and patients usually present in childhood. Occasionally it may present in adulthood. Patients are usually asymptomatic when malrotation of gut is detected during investigations or operation.
Dipankar Ray   +2 more
doaj   +3 more sources

Waugh's Syndrome: Report of Two Children with Intussusception

open access: yesEuropean Journal of Pediatric Surgery Reports, 2017
Waugh's syndrome (WS) is the rare association of intussusception and intestinal malrotation. We present two such cases in a 5-month-old infant and a 9-year-old girl.
Yousuf Aziz Khan   +2 more
doaj   +1 more source

Intestinal Malrotation, Mesocolic Hernia, and Meckel Diverticulum – Differential Diagnosis of Abdominal Pain in Adults: Case Report and Literature Review

open access: yesJournal of Coloproctology, 2021
Intestinal malrotation is a congenital anomaly caused by incomplete rotation or absence of rotation of the primitive intestine along the axis of the upper mesenteric artery during embryonic development. Embryonic development and its anatomical variations
Marcus Vinícius Silva Costa   +5 more
doaj   +1 more source

Segmental volvulus of the ileum without malrotation in an infant: A case report [PDF]

open access: yes, 2011
Intestinal volvulus usually occur secondary to malrotation, and primary segmental volvulus has rarely been reported. A 12-month-old female infant presented with a 3-day history of excessive vomiting.
Dallinga-Thie, Geesje M   +14 more
core   +2 more sources

Predictive factors at birth of the severity of gastroschisis. [PDF]

open access: yes, 2015
To establish children born with gastroschisis (GS). We performed a retrospective study covering the period from January 2000 to December 2007. The following variables were analyzed for each child: Weight, sex, apgar, perforations, atresia, volvulus ...
Ballabeni, P.   +4 more
core   +1 more source

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