Class 3. Pulmonary Hypertension Associated with Lung Hypoplasia Archives

Congenital Hepatopulmonary Fusion in Right Congenital Diaphragmatic Hernia: Surgical Strategyand Outcomes in a Multicenter Cohort

Federica Pederiva, Valerio Gentilimo, Claudio Bonanno, Evelina Bertelli, Laura Morlacchi, Alexandra Benachi, Carmen Mesas Burgos, Luca Giacomello, Paolo Dalena, Matthew T. Harting, and the CHPF study participantsAzienda Ospedaliera Universitaria Integrata. “F. Del Ponte” Hospital. Antoine Béclère Hospital and Paris Saclay University. Karolinska University Hospital and Karolinska Institute. University of Verona. IRCCS “Burlo Garofolo” and University

Congenital Hepatopulmonary Fusion in Right Congenital Diaphragmatic Hernia: Surgical Strategyand Outcomes in a Multicenter Cohort Read More »

Flow versus resistance: hemodynamic phenotyping of pulmonary hypertension in infants with shunts and concurrent lung disease

Tania Gonzalez, Charles T. Simpkin, Paula Dias Maia, Jamie L. Archambault, Anne Taylor, D. Dunbar Ivy, Steven H. Abman, Benjamin S. FrankUniversity of Colorado School of Medicine. Children’s Healthcare of Atlanta and Emory University. United States Frontiers in PediatricsFront Pediatr 2026; 14: DOI: 10.3389/fped.2026.1880632 AbstractNeonatal pulmonary hypertension (PH) can be categorized into three distinct physiologies:

Flow versus resistance: hemodynamic phenotyping of pulmonary hypertension in infants with shunts and concurrent lung disease Read More »

Hemodynamic Phenotypes in Congenital Diaphragmatic Hernia: Unresolved Questions and Future Directions

John T. Wren, Jr., Neil Patel, Patrick J. McNamara, Patrick Sloan University of Iowa, Royal Hospital for Children. Washington University in St. Louis.United States and United Kingdom ChildrenChildren 2026; 13: DOI: 10.3390/children13091137 AbstractCongenital diaphragmatic hernia (CDH) is increasingly recognized as a dynamic cardiopulmonary disease in which pulmonary hypoplasia, pulmonary hypertension, and cardiac dysfunction interact to shape

Hemodynamic Phenotypes in Congenital Diaphragmatic Hernia: Unresolved Questions and Future Directions Read More »

Congenital Diaphragmatic Hernia Guidelines Compliance and Outcomes in Canada

Pramod Puligandla, Robert Baird, Marc Beltempo, Seungwoo Lee, Alexandra Dimmer, Gabriel Altit, Elena Guadagno, Erik SkarsgardMontreal Children’s Hospital and McGill University Health Centre. British Columbia Children’s Hospital. Mount Sinai Hospital and University of Toronto. Canada Journal of Pediatric SurgeryJ Pediatr Surg 2026; DOI: 10.1016/j.jpedsurg.2026.163448 AbstractBackground: Perinatal congenital diaphragmatic hernia (CDH) care in Canada has been

Congenital Diaphragmatic Hernia Guidelines Compliance and Outcomes in Canada Read More »

Alterations of endothelial cell bioenergetics in congenital diaphragmatic hernia

Brian F. Emrick, Irina Zhevlakova, Michael Novotny, Lori Mavrakis, Anny Mulya, Darrell L. Cass, Eiichi Miyasaka, Tatiana V. Byzova, Kewal Asosingh, Serpil C. Erzurum, Jason O. RobertsonCleveland Clinic. Cleveland Clinic Children’s Hospital. University Hospitals Rainbow Babies and Children’s Hospital. United States Pediatric ResearchPediatr Res 2026; DOI: 10.1038/s41390-026-05447-w AbstractBackground: Pulmonary vascular development in congenital diaphragmatic hernia

Alterations of endothelial cell bioenergetics in congenital diaphragmatic hernia Read More »

Cardiac morphology in children at 2 and 10 years of age after congenital diaphragmatic hernia repair: a comparative MRI-based analysis of ECMO and non-ECMO patients

Schanas Jawhar, Greta Thater, Stefan Appelhaus, Michael Boettcher, Julia Elrod, Frank G. Zoellner, Florian Kipfmueller, Marcia Matos Karaorman, Stefan O. Schoenberg, Meike WeisUniversity Medical Center Mannheim, University Children’s Hospital Mannheim and Heidelberg University. Germany European RadiologyEur Radiol 2026; DOI: 10.1007/s00330-026-12841-9 AbstractObjectives: Congenital diaphragmatic hernia (CDH) is a diaphragmatic defect causing lung hypoplasia and frequently resulting in pulmonary

Cardiac morphology in children at 2 and 10 years of age after congenital diaphragmatic hernia repair: a comparative MRI-based analysis of ECMO and non-ECMO patients Read More »

Neonatal Course and Long-Term Outcome in Children With Congenital Chylothorax

N. Beullens, K. Smets, M. De Lausnay, P. Schelstraete, S. Van Daele, J. Willekens, J. Van Dorpe, H. SchaballieGhent University Hospital. Belgium Pediatric PulmonologyPediatr Pulmonol 2026; 61: DOI: 10.1002/ppul.71820 AbstractBackground: Congenital chylothorax is a rare pulmonary developmental disorder with high associated morbidity and mortality. A limited number of cases have been described, and clinical manifestations and outcomes

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Impact of prolonged preterm premature rupture of membranes and oligohydramnios on neonatal outcomes in extremely preterm infants: A nationwide cohort study

Seong Hee Oh, Chan-Hoo Park, Seonok Kim, Byong Sop LeeUniversity of Ulsan College of Medicine and Gangneung Asan Hospital. Gyeongsang National University and Gyeongsang National University Changwon Hospital. University of Ulsan College of Medicine, Asan Medical Center and Children’s Hospital. South Korea Pediatrics and NeonatologyPediatr Neonatol 2026; DOI: 10.1016/j.pedneo.2026.04.011 AbstractBackground: Prolonged preterm premature rupture of membranes (PPROM)

Impact of prolonged preterm premature rupture of membranes and oligohydramnios on neonatal outcomes in extremely preterm infants: A nationwide cohort study Read More »

Bibliometric analysis of congenital diaphragmatic hernia research models: evolution and insights from the past three decades

Boshen Shu, Xiaohui Wang, Richard Wagner, Florian Friedmacher, Martin Lacher, Ophelia AubertHenan Provincial People’s Hospital. University of Leipzig. University Hospital Frankfurt and Goethe University Frankfurt. University Medical Center Mannheim and University of Heidelberg.China and Germany Pediatric Surgery InternationalPediatr Surg Int 2026; 42: DOI: 10.1007/s00383-026-06597-y AbstractBackground: Research models of congenital diaphragmatic hernia (CDH) have evolved over time. We

Bibliometric analysis of congenital diaphragmatic hernia research models: evolution and insights from the past three decades Read More »

A Novel MYRF Variant Presenting With Scimitar Syndrome, Hepatopulmonary Fusion, Right-Sided Congenital Diaphragmatic Hernia, and Uterine Didelphys

Gul Sher, Samantha Weaver, Rahul Adwani, Jai Parkash UdassiWest Virginia University Golisano Children’s Hospital and West Virginia University School of MedicineUnited States Case Reports in PediatricsCase Rep Pediatr 2026; DOI: 10.1155/crpe/8646210 AbstractThe MYRF gene encodes a pleiotropic transcription factor essential for the development of multiple organ systems, including the heart, lungs, diaphragm, and genitourinary tract. Pathogenic variants in MYRF are

A Novel MYRF Variant Presenting With Scimitar Syndrome, Hepatopulmonary Fusion, Right-Sided Congenital Diaphragmatic Hernia, and Uterine Didelphys Read More »