Results 51 to 60 of about 2,259 (155)

Partial urorectal septum malformation sequence with prune belly syndrome and oesophageal atresia with a tracheoesophageal fistula

Journal of Pediatric Surgery Case Reports, 2019
The concurrence of Urorectal Septum Malformation (URSM) Sequence and Prune Belly Syndrome are extremely uncommon, with increased rarity with the coexistence of an oesophageal atresia with tracheoesophageal fistula.
N.Z. Mashavave, D.S. Harrison, A.D. Grieve   +2 more
doaj   +1 more source

Anesthesia‐free transoral endoscopy using a novel modified pacifier in early infancy

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Jonathan A. Berken, Zoe Rosoff‐Verbit, Tyler Babinski, Matthew J. Ryan, the Transpacifier Endoscopy Research Group, Elizabeth Silvestro, Michael A. Manfredi   +6 more
wiley   +1 more source

Facilitating Genetic Testing for Perinatal Demise: Development of a Multidisciplinary Workflow

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1273-1285, June 2026.
ABSTRACT Genetic contributors to perinatal demise are common but frequently undiagnosed due to clinical and logistical barriers. We aimed to improve access to genetic for intrauterine fetal demise (IUFD), stillbirth, and early neonatal death by developing a multidisciplinary workflow.
Mackenzie Mosera, Samantha Stover, Elise Boos, Molly Casey, Joseph Fanning, Chelsea Fechter, Matthew Grace, L. Dupree Hatch, Michaela Ibach, Carla Jackson, Jiancong Liang, Caitlin Mann, Emily A. Morris, Jessica Turnbull, Marie Williams, Bryce A. Schuler   +15 more
wiley   +1 more source

Pierre Robin sequence in association with tracheoesophageal fistula and esophageal atresia

, 2019
The first symptom of esophageal atresia and tracheoesophageal fistula is the inability to eat and respiratory distress after feeding. The coexistence of Pierre Robin Sequence (PRS) with esophageal atresia and tracheoesophageal fistula is a rare clinical ...
Baltrak, Yusuf Atakan, Varlikli, Onursal
core   +2 more sources

Unsuccessful Intubation and Stabilization by Laryngeal Mask Airway in the Delivery Room: A Case of Tracheal Atresia

Case Reports in Pediatrics, 2021
A term male newborn infant was apneic at birth, and endotracheal intubation was unsuccessful. He was stabilized for transport with a laryngeal mask airway. Laryngoscopy revealed tracheal atresia with intrathoracic distal tracheoesophageal fistula.
Mark Cody Smith, Autumn Kiefer, C. Eric Bailey   +2 more
doaj   +1 more source

Determinants of Healthcare Costs in Individuals With Down Syndrome: A Systematic Review

Health Science Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Background Individuals with Down syndrome (DS) require specialized medical follow‐up and services more frequently than the general population, resulting in substantial healthcare costs for families and health systems. This systematic review aimed to synthesize evidence on the magnitude and determinants of direct healthcare and indirect costs ...
Shiva Tolouei Rakhshan, Sarah Byford, Mahya Razimoghadam, Fardin Moradi, Shahin Soltani   +4 more
wiley   +1 more source

SURGICAL OUTCOME OF 65 CASES OF CONGENITAL ESOPHAGEAL ATRESIA WITH TRACHEOESOPHAGEAL FISTULA: EXPERIENCE OF 5 YEARS IN TWO INSTITUTES

The Iraqi Journal of Medical Sciences, 2016
Background:Congenital esophageal atresia and tracheoesophageal fistula are well-known congenital anomalies which affect 1 in 2400 – 4500 live births.
Ahmed Z. Zain, Salah S. Mahmood, Sarah Z. Fadhil   +2 more
doaj   +4 more sources

Persistent Pulmonary Atelectasis After Tracheoesophageal Fistula Repair: Diagnostic Challenge of a Communicating Bronchopulmonary Foregut Malformation Group 1a in a Neonate With VACTERL Association

The Kaohsiung Journal of Medical Sciences, EarlyView.
Tien‐Pai Huang, Twei‐Shiun Jaw, Yu‐Tang Chang, Yu‐Han Chen   +3 more
wiley   +1 more source

Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study

Journal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 6, Page 1386-1393, June 2026.
Abstract Objective To evaluate neurodevelopment at 24 months in infants surgically treated for esophageal atresia (EA), using the ages and stages questionnaire (ASQ), and identify perinatal and early‐life factors associated with developmental delay. Methods Infants with EA were prospectively enrolled in a structured multidisciplinary follow‐up program.
Julia Tagmouti, Manon Midavaine, Victor Sartorius, Nicolas Vinit, Elise Leroy‐Terquem, Sylvie Beaudoin, Elsa Kermorvant‐Duchemin, Véronique Rousseau, Alexandre Lapillonne   +8 more
wiley   +1 more source

Congenital Pulmonary Airway Malformations in Children: Beyond the Pulmonary Cystic Lesion Is There Really an Associated Laryngo‐Tracheal Abnormality?

Pediatric Pulmonology, Volume 61, Issue 6, June 2026.
ABSTRACT Background Congenital pulmonary airway malformations (CPAMs) are rare developmental anomalies of the lower respiratory tract. Although their pulmonary and postnatal respiratory implications are well recognized, the possible coexistence of laryngotracheal abnormalities remains poorly investigated.
Antonio Mario Bulfamante, Ugo Maria Pierucci, Giorgio Imbrogno, Lydia Alejandra Olaya Leon, Gloria Pelizzo   +4 more
wiley   +1 more source