Results 31 to 40 of about 83,842 (143)
Foker technique for esophageal reconstruction after cervical esophagostomy
The approach to patients with complicated esophageal atresia continues to be a challenge for the pediatric surgeon. Patients with long-gap esophageal atresia (LGEA) or who had complications during their first surgery may require cervical esophagostomy ...
Giovana Camargo de Almeida +3 more
doaj +1 more source
Diagnostic challenge of concomitant small bowel atresia and Hirschsprung's disease
The incidence of ileal atresia ranges from 1/5000 to 1/12000 births. The incidence of Hirschsprung's disease is 1/5000.The combination of Hirschsprung disease and ileal atresia during infancy seems to be a rare event and the exact incidence of the ...
I. Belbahri +6 more
doaj +1 more source
Apple Peel Deformity and Malrotation of Gut: Autopsy Findings of a Rare Cause of Mortality in Utero
One-third of all intestinal obstructions in the newborn are caused by atresias. The most common site is the duodenum followed by jejunoileal and colonic locations.
Deepti MUTREJA, Sharanjit SINGH
doaj +1 more source
Congenital diseases of the large intestine of dogs and cats have scarcely been reported and mostly include fistula, atresia or colonic duplication. Cases of partial colonic agenesis have rarely been described.
Paul Remmel +3 more
doaj +1 more source
Different varieties of colonic atresia in a series of 13 patients: a single-center experience [PDF]
Purpose The aim of this study was to review our experience in the management and outcome of colonic atresia, either isolated or associated with anorectal anomalies.Methods A total of 13 neonates with colonic atresia were operated upon in the Pediatric ...
Khalifa, M, Gobran, TA, Kamal, RMK
core +1 more source
Colonic atresia: The rarest atresia of the gastrointestinal tract
Colonic atresia (CA) is a rare cause of intestinal obstruction of the newborn. It is the rarest atresia of the gastrointestinal tract. The survival rate is 90%. However, the delayed diagnosis and surgery after 72 hours of life, have a high mortality rate.
Molinaro F. +6 more
core +2 more sources
Congenital absence of small bowel with anorectal malformation
We report a unique case of congenital absence of small bowel with associated anorectal malformation and duodenal atresia. Currently, there is no report of a similar case in a live infant in the literature.
Irene Isabel P. Lim, MD, MPH +1 more
doaj +1 more source
Congenital segmental dilatation of ascending colon with distal microcolon: A diagnostic dilemma
A 5-day-old male presented with bilious vomiting, a grossly distended abdomen, and passage of a small amount of stool. The anal opening was at a normal position.
Ruchira Nandan +4 more
doaj +1 more source
Aim. Development of methodology that would allow surgeons to decrease the risk of colo-esophageal anastomotic dehiscence following esophagoplasty through prevention of colonic transplant compression in the retrosternal tunnel and surgery facilitation ...
A. N. Kivva +6 more
doaj +1 more source
Despite the increasing incidence of gastroschisis, the cause remains unknown. Genetic factors may contribute to bowel anomalies as demonstrated by cases of gastroschisis in twins and siblings, and other types of bowel anomalies in twins.
Saxonhouse, Matthew A +4 more
core +1 more source

