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 […]
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,
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
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
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
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
Ryan D. Coleman, Sarah P. Cohen, Pirooz Eghtesady, R. Mark Grady, David L. S. Morales. Don Hayes Jr., Joseph K. Ruminjo, W. Graham CarlosBaylor College of Medicine. Nationwide Children’s Hospital. Washington University School of Medicine. Cincinnati Children’s Hospital Medical Center. Indiana University School of Medicine. United States Annals of the American Thoracic SocietyAnn Am Thorac
Piero Alberti, Niyi Ade-Ajayi, Anne GreenoughKing’s College London.United Kingdom ChildrenChildren 2025; 12: DOI: 10.3390/children12030273 AbstractNeonates with congenital conditions which require surgical management frequently experience respiratory distress. This review discusses the management of pulmonary complications and the respiratory support strategies for four conditions: oesophageal atresia-tracheoesophageal fistula (OA-TOF), congenital diaphragmatic hernia (CDH), congenital lung malformations (CLM), and anterior
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Dina Al Namat, Romulus Adrian Ros, Razan Al Namat, Elena Hanganu, Andrei Ivan, Delia Hînganu, Ancut Lupu, Marius Valeriu HînganuUniversity of Medicine and Pharmacy “Grigore T. Popa”. “Saint Mary” Emergency Children HospitalRomania DiagnosticsDiagnostics 2025; 15: DOI: 10.3390/diagnostics15060675 AbstractOmphalocele is a rare congenital abdominal wall defect, occurring in approximately 3.38 per 10,000 pregnancies. It is characterized by
Bibhuti B. Das, Shashi RajUniversity of Mississippi Medical Center. Narayana Health.United States and India Journal of Heart and Lung Transplantation OpenJHLT Open 2025; 7: DOI: 10.1016/j.jhlto.2024.100203 AbstractRight ventricular failure (RVF) is a clinical syndrome resulting from structural and functional changes in the right ventricle (RV), leading to inadequate blood flow to the pulmonary circulation and elevated
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