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The Role of Genetics in Congenital Heart Disease-Associated Pulmonary Arterial Hypertension

Fatma Hayvaci Canbeyli, Kazim Secgen, Faith Suheyl Ezgu, Gulten Tacoy, Serkan Unlu, Hidayet Ozan Arabaci, Ayhan Pektas, Asli Inci, Ergun Baris Kaya, Umit Yasar Sinan, Mehmet Serdar Kucukoglu, Serdar KulaGazi University Faculty of Medicine. Istanbul University Faculty of Medicine. Afyonkarahisar University of Health Sciences. Hacettepe University Faculty of Medicine. Turkey Pediatric CardiologyPediatr Cardiol 2025; DOI: 10.1007/s00246-025-03847-z […]

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Complete Atrioventricular Septal Defect Repair in Patients With Down Syndrome Presenting Beyond Six Months- A Single Center Experience

Kartik Patel, Chandrasekaran Ananthanarayanan, Trushar Gajjar, Amit Mishra, Bhavik Champaneri, Jigar Surti, Himani PandyaU. N. Mehta Institute of Cardiology and Research Centre. India World Journal of Pediatric and Congenital SurgeryWorld J Pediatr Congenit Surg 2025; DOI: 10.1177/21501351251322162 AbstractBackground: Complete atrioventricular septal defect (cAVSD) is the most common cardiac lesions associated with Down syndrome (DS). In DS,

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Cellular Communication Network Protein 2 in the Right Ventricle of Pulmonary Arterial Hypertension

Carly E. Byrd, Jennifer E. Schramm, Jun Yang, Allan E. Barnes, Megan Griffiths, Anjira S. Ambade, Darin T. Rosen, Ilton M. Cubero Salazar, Catherine E. Simpson, Ryan J. Tedford, Steven Hsu, Dhananjay Vaidya, Todd M. Kolb, Michael W. Pauciulo, William C. Nichols, David D. Ivy, Eric D. Austin, Paul M. Hassoun, Rachel L. Damico, Allen

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Evaluating Frequency and Yield of Echocardiography in a Pediatric Intensive Care Unit

Shafee Salloum, Andrew J. Lautz, MD, Christopher StatileCincinnati Children’s Hospital Medical Center and University of Cincinnati College of Medicine.United States Journal of Pediatrics. Clinical PracticeJ Pediatr Clin Pract 2025; 16: DOI: 10.1016/j.jpedcp.2025.200143 AbstractObjective: To evaluate the frequency and diagnostic yield of transthoracic echocardiography (TTE) in a noncardiac pediatric intensive care unit (PICU).Study design: This was a single-center retrospective

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Characteristics and sex differences in bronchopulmonary dysplasia-related pulmonary hypertension

Dansha Zhou, Ting Wang, Yuqin Chen, Yulin Zheng, Yingzhen Zhou, Mingxiang Zhang, Aofeng Liu, Biao Hu, Shuang Fu, Ruixian Wu, Wei Chen, Xiaoli Jiang, Zehui Ye, Yuan Shi, Zhou Fu, Jian WangFirst Affiliated Hospital of Guangzhou Medical University and Guangzhou Medical University. Children’s Hospital of Chongqing Medical University. China BioMedical Central Pulmonary MedicineBMC Pulm Med

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Eliglustat and cardiac comorbidities in Gaucher disease: a pharmacogenomic approach to safety and efficacy

Noor Ul Ain, Armaan Saith, Audrey Ruan, Ruhua Yang, Aaron Burton, Pramod K. MistryYale School of Medicine and Yale New Haven Hospital.United States Frontiers in MedicineFront Med 2025; 12: DOI: 10.3389/fmed.2025.1535099 AbstractIntroduction: Gaucher disease (GD), a lysosomal storage disorder, results from the accumulation of glycosphingolipids due to deficient lysosomal glucocerebrosidase activity. This pathological accumulation triggers immune activation,

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Mechanisms of hypoxaemia in late pulmonary hypertension associated with bronchopulmonary dysplasia

Eleanor Jeffreys, Fahad M. S. Arattu Thodika, Aaron Bell, Anne Greenough, Theodore DassiosKing’s College, King’s College Hospital and NHS Foundation Trust. Evelina Children’s Hospital, Guy’s and St Thomas’ NHS Foundation Trust. University of Patras.United Kingdom and Greece Journal of Perinatal MedicineJ Perinat Med 2025; DOI: 10.1515/jpm-2025-0058 AbstractAbstract Not Available CategoryClass III. Pulmonary Hypertension Associated with Lung

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Left Innominate Artery With Anomalous Origin From the Pulmonary Trunk: A Case Report of an Unnoticed Malformation

Juan D. Ayala Torres, Marcia Mejía Velasquez, Mónica Royero-AriasUniversidad de Antioquia. Clínica las Américas. Servicios de Salud San Vicente Fundación.Columbia CureusCureus 2025; 17: DOI: 10.7759/cureus.79661 AbstractThoracic vascular congenital anomalies are malformations with significant clinical implications. One of the rarest anomalies is the anomalous origin of the brachiocephalic trunk from the pulmonary trunk, often associated with serious

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Nasopharyngeal ventilation: an answer to the conundrum of severe nasal injury in a neonate

Bhabesh Kant Chowdhry, Arnab Ghorui, Richie Dalai, Rameshwar PrasadAll India Institute of Medical Sciences.India British Medical Journals Case ReportsBMJ Case Rep 2025; 18:DOI: 10.1136/bcr-2025-264797 AbstractA term neonate with a stormy perinatal course, requiring prolonged mechanical ventilation, due to congenital pneumonia, complicated by secondary pulmonary arterial hypertension and prolonged non-invasive respiratory support, presented to us in the

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Pathogenic Concepts in Pulmonary Arterial Hypertension Revisited – A Multigenerational Perspective

Graznya Kwapiszewska, Christopher Rhodes, Marlene Rabinovitch, Catherine Simpson, Paul Hassoun, Kenzo Ichimura, Marc Humbert, Edda SpiekerkoetterMedical University Graz. Imperial College London. Stanford University. Johns Hopkins University. Hopital Bicetre. Austria, United Kingdom, United States and France American Journal of Respiratory Cell and Molecular BiologyAm J Respir Cell Mol Biol 2025; DOI: 10.1165/rcmb.2024-0519PS AbstractThe rapid advancement of next-generation

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