Results 1 to 10 of about 11,497 (209)

A case of congenital total intestinal atresia in a neonate: a case report [PDF]

open access: yesJournal of Medical Case Reports
Introduction Intestinal atresia is the complete occlusion of the intestinal lumen at various parts of the intestine. It has the potential to cause intestinal failure. Two mechanisms are suggested: failure of recanalization and/or accidental injury.
Hindeya Hailu Hagos   +5 more
doaj   +2 more sources

Primary Repair of a Jejunal Atresia With Christmas Tree Deformity in a Preterm Infant [PDF]

open access: yesClinical Case Reports
Although uncommon in the general population, jejunoileal atresia (JIA) is a common cause of intestinal obstruction in infants. This congenital anomaly may cause a substantial reduction in intestinal length, enhancing the likelihood of short bowel ...
Dennis Machaku   +5 more
doaj   +2 more sources

Intestinal atresia in twins

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Intestinal atresia is a congenital anomaly which results in the discontinuity or narrowing of the bowel lumen. Although intestinal atresia is a common congenital malformation, it rarely occurs in twins.
Lucas Fair, Brett Johnson, John Uffman
doaj   +1 more source

Histomorphological Features of Intestinal Atresia and its Clinical Correlation [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Introduction: Intestinal atresia accounts for approximately one third of all cases of neonatal intestinal obstruction. There is controversy regarding pathogenesis of congenital atresia and stenosis of small bowel.
Devi Subbarayan   +3 more
doaj   +1 more source

A Rare Case of Jejunal Atresia Due to Intrauterine Intussusception [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Intestinal atresia is generally caused by intrauterine vascular obstructions involving mesenteric vessels. Intrauterine intussusceptions (IUI) are one of these disruptive events. Intestinal intussusceptions affects children commonly between 3 months and
Sanjeev B Joshi   +4 more
doaj   +1 more source

Apple-peel intestinal atresia treated by diamond-shaped anastomosis to adjust the anastomosis size

open access: yesJournal of Pediatric Surgery Case Reports, 2022
An apple-peel intestinal atresia is a rare form of bowel atresia. Herein, reported a case of apple-peel intestinal atresia that was treated with a diamond-shaped anastomosis to adjust the anastomosis size.
Yuki Muta   +3 more
doaj   +1 more source

Congenital multiple colonic atresias with intestinal malrotation: a case report

open access: yesSurgical Case Reports, 2020
Background Congenital intestinal atresia develops in 1 in 1500 to 20,000 births. Colonic atresia, which accounts for 1.8–15% of intestinal atresia cases, is accompanied by other gastrointestinal atresias such as small intestinal atresia, gastroschisis ...
Daisuke Ishii   +3 more
doaj   +1 more source

Congenital band causing small bowel obstruction in a newborn

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Introduction: Intestinal atresia refers to a complete obstruction of the bowel lumen. Anomalous congenital bands are rarely found as causes of intestinal obstruction in children. Most congenital bands occur in the small intestine.
Mariam Marzouki   +7 more
doaj   +1 more source

Late presentation of incomplete jejunal atresia

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Intestinal atresia is a life-threatening cause of intestinal obstruction in the neonate, and rarely a cause of intestinal obstruction in an infant. We report a rare presentation of an incomplete jejunal atresia in a 1-year and 7 months old girl.
Elroy P. Weledji   +2 more
doaj   +1 more source

Monozygotic twins with jejuno-ileal atresia

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Introduction: Intestinal atresia is a congenital anomaly of the alimentary canal characterised by discontinuity of the bowel lumen that leads to intestinal obstruction in neonates.
Dennis Mazingi   +8 more
doaj   +1 more source

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