Results 31 to 40 of about 21,575 (142)
Embryogenesis of esophageal atresia: Is localized vascular accident a factor?
Several theories on embryogenesis of esophageal atresia have been proposed, none could explain the whole spectrum of this anomaly. We report a new variant of esophageal atresia in which the two blind pouches were joined by an atretic band.
Dutta Hemonta, Harsh Shree
doaj +1 more source
Neurodevelopmental outcomes among children with congenital gastrointestinal anomalies using Korean National Health Insurance claims data [PDF]
This study investigated neurodevelopment and risk factors in children surgically treated for congenital gastrointestinal anomalies (CGIA), excluding those with known high-risk factors such as low birth weight or chromosomal anomalies.
Hannah Cho +4 more
doaj +2 more sources
Abstract Background Enteral drug therapy is challenging in short bowel syndrome with intestinal failure (SBS‐IF) because of unpredictable absorption. SEFA‐6179 is an enterally administered medium‐chain fatty acid analogue under development for intestinal failure–associated liver disease. We investigate the pharmacokinetics of two SEFA‐6179 formulations
Scott C. Fligor +9 more
wiley +1 more source
Congenital small bowel obstruction: Prenatal detection and outcome
Abstract Objective To evaluate and compare the outcome of fetuses and neonates with congenital small bowel obstructions (SBO), evaluate the screening performance of prenatal ultrasound for SBO and identify possible risk factors for adverse outcomes.
H. Heinrich +6 more
wiley +1 more source
Ileal atresia and total colonic hirschsprung disease in a 36‐week neonate: A case report
Colonic aganglionosis should be in mind in any operated infant with small intestinal atresia repair who continues to exhibit poor bowel function after corrective surgery. Abstract Intestinal atresia and hirschsprung disease are two common causes of bowel obstruction in neonates; simultaneous occurrence is rare.
Khashahyar Atqiaee +3 more
wiley +1 more source
Abstract The beta‐actin gene (ACTB) encodes a ubiquitous cytoskeletal protein, essential for embryonic development in humans. De novo heterozygous missense variants in the ACTB are implicated in causing Baraitser–Winter cerebrofrontofacial syndrome (BWCFFS; MIM#243310). ACTB pathogenic variants are rarely associated with intestinal malformations.
Kristina Sibbin +11 more
wiley +1 more source
Atresia Jejunoileal grau IV em neonato: relato de caso [PDF]
Uma grande variedade de anormalidades congênitas pode atingir qualquer porção do trato gastrointestinal, desde o esôfago ao anus. A atresia é a mais comum causa de obstrução intestinal congênita, com uma elevada taxa de morbidade em recém-nascidos.
de Bittencourt, Luiza La Rocca Ganho +7 more
core +1 more source
Changes of smooth muscle contractile filaments in small bowel atresia [PDF]
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
Jejunoileal Atresia A study of 60 cases in children welfare teaching hospital.
Background: Congenital defects in continuity of the intestine are morphologically divided into either stenosis or atresia and constitute one of the most common causes of neonatal intestinal obstruction.
Ahmed A. Khalaf +2 more
doaj +1 more source
JPGN Reports, Volume 3, Issue 1, February 2022.
Andrea Gosalvez‐Tejada +5 more
wiley +1 more source

