Fresh (PHresh). Less than 1-2 years since publication

Echocardiographic Analysis of Missed and Misdiagnosis in Children With Anomalous Origin of the Left Coronary Artery From the Pulmonary Artery

Zhen Cheng, Changbai Ding, Shanliang Zhu, Hao Liu, Yu Mao, Ying Tang, Chenshuang Zhou, Jun ChenNanjing Gaochun People’s Hospital. People’s Hospital of Pizhou. Children’s Hospital of Nanjing Medical University.China Journal of Clinical UltrasoundJ Clin Ultrasound 2026; DOI: 10.1002/jcu.70352 AbstractObjective: To evaluate the practical application of echocardiography in identifying anomalous left coronary artery from the pulmonary artery (ALCAPA)

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Unusual Clinical Course of Pediatric Pulmonary Hypertension with Underlying SOX17 Mutation

Aldana Rojas, David L. S. Morales, Kathryn A. Wikenheiser-Brokamp, Don Hayes Jr.Cincinnati Children’s Hospital Medical Center and University of Cincinnati.United States Annals of the American Thoracic SocietyAnn Am Thorac Soc 2026; DOI: 10.1093/annalsats/aaoag216 AbstractAbstract Not Available CategoryClass I. Heritable Pulmonary HypertensionGenetic Factors Associated with Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed

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Echocardiography Assessment of Cardiac Function and Pulmonary Hypertension in Lambs

Yasmine N. White, Matthew Douglass, Reagan Cathcart, Jakob Van Boerum, Andrew Rebentisch, Kurt H. Albertine, Marjanna DahlUniversity of Utah.United States Journal of Visualized ExperimentsJ Vis Exp 2026; DOI: 10.3791/70686 AbstractPremature birth is strongly associated with cardiac dysfunction, including impaired ventricular function and altered cardiac structure, which can lead to progressive heart failure and other short- and

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Familial Hereditary Hemorrhagic Telangiectasia with Stroke in Two Generations: Diagnostic Delay and the Role of Patient-Specific Three-Dimensional-Printed Models in Endovascular Planning

Ke-Yun Chao, Chao-Yu Chen, Yi-Zhen Chu, Hng-Ka Lm, Shu-Chi Mu, Yu-Hsuan ChienFu Jen Catholic University College of Medicine. National Taiwan University Hospital Yunlin Branch. Shin Kong Wu Ho-Su Memorial Hospital. Taiwan Acta Cardiologica SinicaActa Cardiol Sin 2026; 42: 645-648DOI: 10.6515/ACS.202607_42(4).20260411A AbstractAbstract Not Available CategoryPulmonary Arteriovenous MalformationsDiagnostic Testing for Pulmonary Vascular Disease. Non-invasive TestingSurgical and Catheter-mediated Interventions

Familial Hereditary Hemorrhagic Telangiectasia with Stroke in Two Generations: Diagnostic Delay and the Role of Patient-Specific Three-Dimensional-Printed Models in Endovascular Planning Read More »

Transoesophageal echocardiography following ventricular septal defect repair: A retrospective case series on the upcoming role of right ventricular-pulmonary arterial uncoupling

Rohan Magoon, Tanya Mital, Jasvinder K. Kohli, Ravi Bathia, Naman JainAtal Bihari Vajpayee Institute of Medical Sciences (ABVIMS) and Dr. Ram Manohar Lohia Hospital. India Journal of Anaesthesiology Clinical PharmacologyJ Anaesthesiol Clin Pharmacol 2026; 42: 437-440DOI: 10.4103/joacp.joacp_46_26 AbstractThe role of right ventricular (RV)-pulmonary arterial (PA) coupling is being increasingly recognized, with the ratio of tricuspid annular

Transoesophageal echocardiography following ventricular septal defect repair: A retrospective case series on the upcoming role of right ventricular-pulmonary arterial uncoupling Read More »

Survival Into Adulthood With FOXF1-Associated Pulmonary Vascular Disease After Neonatal Onset

Khalifah A. Aldawsari, Steven H. Abman, David Badesch, David Dunbar IvyUniversity of Colorado Anschutz Medical School and Children’s Hospital Colorado. United States Pulmonary CirculationPulm Circ 2026; 16: DOI: 10.1002/pul2.70378 AbstractNeonates and infants with FOXF1 mutation develop alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV), which is typically considered a uniformly fatal neonatal lung disorder due

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Pulmonary Hypoplasia

Aneesha Geraghty, Patrick Smith, Kristen Arnold, Paul S. KingmaUniversity of Cincinnati College of Medicine and Cincinnati Children’s Hospital Medical Center.United States NeoReviewsNeoreviews 2026; 27: e511-e522DOI: 10.1542/neo.27-7-039 AbstractPulmonary hypoplasia is a rare but clinically significant congenital disorder characterized by impaired fetal lung development, leading to impaired growth and maturation of lung parenchyma and pulmonary vasculature. Stemming from

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Pilot study to validate endothelium collection from pulmonary artery balloon catheter in children

Maxwell Mathias, Charles Sperrazza, Anas Salkini, Andrew Cave, Courtney T. Griffin, Venkatachalem Sathish, Subhrajit LahiriUniversity of Oklahoma Health College of Medicine. Oklahoma Medical Research Foundation. United States Pediatric ResearchPediatr Res 2026; DOI: 10.1038/s41390-026-05326-4 AbstractPediatric pulmonary hypertension (PH) has high morbidity and mortality, with an estimated 5-year survival of 75% regardless of underlying cause. Pediatric PH most

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Post-translational modification crosstalk in pulmonary arterial hypertension: mechanisms and therapeutic implications

Jialin Liang, Yuxin Xie, Danyan Su, Yusheng Pangirst Affiliated Hospital of Guangxi Medical University. Guangxi University of Chinese Medicine. China Molecular Biology ReportsMol Biol Rep 2026; 53: DOI: 10.1007/s11033-026-12478-3 AbstractPulmonary arterial hypertension (PAH) is a complex vascular disease characterized by endothelial dysfunction, pulmonary arterial smooth muscle cell (PASMC) hyperproliferation, metabolic reprogramming, and immune-inflammatory remodeling. These pathological

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Identification of Clinical Sub-Phenotypes of Sickle Cell Disease Using Latent Class Analysis

Shaina M. Willen, Ann M. Brunson, Oyebimpe O. Adesina, Ted WunUniversity of California Davis. United States American Journal of HematologyAm J Hematol 2026; DOI: 10.1002/ajh.70459 AbstractSickle cell disease (SCD), a monogenic disorder, exhibits variable severity due to genetic and environmental modifiers. Prior studies have proposed hemolytic and vaso-occlusive sub-phenotypes based on limited data. We used latent

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