Results 41 to 50 of about 61,174 (158)

Cholangitis and Choledocholithiasis After Repair of Duodenal Atresia: A Case Report [PDF]

Acta Medica Iranica, 2011
Cholelithiasis is a rare but known complication of surgery for duodenal atresia. Occurrence of choledocholithiasis as sequelae of duodenoduodenostomy is still rarer. Biliary stasis resulting from compression of common bile duct due to periductal fibrosis
Atia Zaka-ur-Rab, Zeeba Zaka-ur-Rab, Rehan Fareed, Intezar Ahmed   +3 more
doaj   +2 more sources

Single-stage surgical repair of a preterm neonate with congenital triple atresia: a case report

Journal of Pediatric Surgery Case Reports
Introduction: Congenital triple atresia involving esophageal atresia/tracheoesophageal fistula, duodenal atresia and anorectal malformation is an exceptionally rare association, with limited evidence guiding optimal surgical timing and staging.
Kevin Teerovengadum, Subha Shita Devi Gaya, Kenigen Manikion, Jethishka Motee, Faeza Bibi Soobadar   +4 more
doaj   +1 more source

Anomalous pancreatic ductal system allowing distal bowel gas with duodenal atresia

Journal of Pediatric Surgery Case Reports, 2017
A twelve-day-old male presented with non-bilious, non-bloody emesis 2 hours after feeding since two-days-old, with flatus and light stools since birth. An upper gastrointestinal series (UGI) at an outside institution was reported as normal.
Shruti Sevak, Begum Akay, David A. Bloom
doaj   +1 more source

Duodenal atresia with apple peel jejunoileal syndrome

Journal of Pediatric Surgery Case Reports, 2021
Embryologically, duodenal atresia results from inadequate recanalization and proliferation of the solid cord in the 8–10th week of gestation, while apple-peel atresia is a consequence of a vascular accident.
Taís Wong, Fábio Volpe, Md F.G. Tazima, W.C. Canesin, Lourenço Sbragia   +4 more
doaj   +1 more source

Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 1953-1972, September 2026.
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll, Yves Alembik, Marie‐Paule Roth   +2 more
wiley   +1 more source

Duodenal Atresia Repair: A Single-Center Comparative Study.

, 2023
BACKGROUND: The use of laparoscopy in the repair of duodenal atresia has been increasing. However, there is no consensus regarding which surgical approach has better outcomes. We aimed to compare the different surgical approaches and types of anastomoses
Cruz-Centeno, Nelimar, Marlor, Derek R, Rentea, Rebecca M, Snyder, Charles L, Fraser, Jason D, Oyetunji, Tolulope A, MD MPH, Hendrickson, Richard J, Aguayo, Pablo, Juang, David, St Peter, Shawn D, Stewart, Shai   +10 more
core   +1 more source

Identification of major congenital malformations based on healthcare databases in France: A proof‐of‐concept study using the epi‐meres nationwide mother–child register

British Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 3037-3048, September 2026.
Abstract Aim Besides registries, healthcare databases can provide useful information for assessing the frequency of major congenital malformations (MCMs) and investigating their risk factors, particularly medication exposures. This study aimed to assess the validity of MCMs identification based on French national, comprehensive healthcare databases ...
Tom Duchemin, Lise Marty, Jérôme Drouin, Sara Miranda, Jérémie Botton, Valérie Olié, Alain Weill, Rosemary Dray‐Spira   +7 more
wiley   +1 more source

Situs inversus abdominalis and duodenal atresia [PDF]

, 2016
Fewer than 20 patients born with situs inversus and duodenal atresia have been reported in the literature. We present a patient with this condition. A newborn baby presented shortly after birth with persistent bilious vomiting.
Sidler, Daniel, Rode, Heinz, Brown, Craig, Numanoglu, Alp   +3 more
core   +1 more source

Suppression of Helicobacter pylori reduces gastrin releasing peptide stimulated gastrin release in duodenal ulcer patients. [PDF]

, 1992
Helicobacter pylori increases gastrin release in duodenal ulcer patients. This may be through disruption or changes in the mucus layer affecting the access of luminal stimulants to gastrin releasing cells.
Ghosh, P, Levi, S, Calam, J, Beardshall, K, Moss, S, Gill, J, Playford, RJ   +6 more
core   +4 more sources

Biliary atresia with splenic malformation with associated ductal plate malformation and duodenal atresia: A case report

Indian Journal of Pathology and Microbiology
Biliary atresia (BA) is the most common cause of the obstructive type of neonatal cholestasis that requires prompt surgical intervention. About 10% of neonates with BA have other congenital anomalies, of which splenic malformation (BASM) is a well-known ...
Raktim Mukherjee, Aniket Halder, Suman Kumar Das, Suchandra Mukherjee, Uttara Chatterjee   +4 more
doaj   +1 more source