Results 21 to 30 of about 83,842 (143)
Frontiers in Pediatrics, 2022 Jejunoileal atresia (JIA) is one of the common etiologies of intestinal obtrusion in neonates. However, cases of concomitant ileal atresia and Hirschsprung disease (HD) rarely occur.
Bassam N. AlBassam +6 more
doaj +1 more source
Congenital multiple colonic atresias with intestinal malrotation: a case report
Surgical 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
Changes of smooth muscle contractile filaments in small bowel atresia [PDF]
, 2012 AIM: To investigate morphological changes of intestinal smooth muscle contractile fibres in small bowel atresia patients. METHODS: Resected small bowel specimens from small bowel atresia patients (n = 12) were divided into three sections (proximal ...
Rolle, Udo +4 more
core +1 more source
Colonic atresia and anorectal malformation in a Haitian patient: a case study of rare diseases. [PDF]
Springerplus, 2014 Introduction: Colonic atresia and anorectal malformation are rare congenital anomalies individually. Few reports of the conditions combined in a single patient have been published in the literature.
Derenoncourt MH +5 more
europepmc +2 more sources
Jejunoileal atresias associated with colonic atresia
Journal of Pediatric Surgery Case Reports, 2020 Colonic atresia (CA) is one of the rarest causes of neonatal intestinal obstruction. The combination of jejunoileal atresia (JIA) and CA is particularly rare.
Hiroshi Hamada +3 more
doaj +1 more source
Type II Colonic Atresia and High Anorectal Malformation: A Rare Coexistence and Literature Review [PDF]
Indian Journal of Neonatal Medicine and Research, 2017 Colonic atresia and anorectal malformation are congenital anomalies affecting distal gastrointestinal tract. Individually, both the anomalies need urgent surgical and medical care for survival of the newborn.
Prasanta Kumar Tripathy +1 more
doaj +1 more source
Ileal atresia and total colonic hirschsprung disease in a 36‐week neonate: A case report
Clinical Case Reports, 2023 Intestinal atresia and hirschsprung disease are two common causes of bowel obstruction in neonates; simultaneous occurrence is rare. This report delineates a 36‐week newborn with ileal atresia and total colonic hirschsprung who was referred to our unit ...
Khashahyar Atqiaee +3 more
doaj +1 more source
Congenital multiple colonic atresias in the sigmoid colon and upper rectum
Journal of Pediatric Surgery Case Reports, 2023 Introduction: Congenital colonic atresia develops in 1 in 20,000 to 66,000 births, accounting for 1.8–15% of all intestinal atresias. Approximately 8.9% of patients with colonic atresia have multiple colonic atresias.
Kai Konishi +5 more
doaj +1 more source
Double Atresia of the Hindgut with Ileal Stenosis: A Case Report
Asian Journal of Surgery, 2004 An unusual case of imperforate anus with sigmoid colonic atresia and ileal stenosis is described. Only six cases of imperforate anus associated with colonic atresia have previously been reported in Japan.
Koushi Asabe, Akira Nagasaki
doaj +1 more source
Fenestrated Colonic Atresia: A rare presentation
Journal of Pediatric Surgery Case Reports, 2020 Congenital Colonic Atresia is described to be the rarest form of intestinal atresia and many anomalies can be associated with it. Surgical repair is the definitive treatment but managing it with primary anastomosis vs intestinal diversion is still being ...
Mohamad H. El Mahmoud +2 more
doaj +1 more source