Symptoms and Findings Associated with Pulmonary Vascular Disease

Pediatric pulmonary hypertension registry: Single-center experience from India

Wadile Santosh, Mishra Arpita, Banpurkar Ashishkumar Moreshwar, Raeen Shahena Parveen, Kulkarni SnehalSri Sathya Sai Sanjeevani Centre for Child Heart Care and Training in Pediatric Cardiac Skills.India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2026; 19: 14-22DOI: 10.4103/apc.apc_181_24 AbstractBackground: Pulmonary hypertension (PH) is a rare and usually irreversible disease, eventually leading to right heart failure (RHF). There are multiple […]

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Case Report: Cor triatriatum sinister presenting as acute decompensated heart failure in an adolescent

ZainEdeen Zyadah, Joyce Morcos, Alaa Alresheq, Salem K. Qupp, Ahmad Fatayer, Jahed BushnaqAl-Quds University. Palestine Medical Complex. Washington University of Health and Science.Palestine and Belize Frontiers in Cardiovascular MedicineFront Cardiovasc Med 2026; 13: DOI: 10.3389/fcvm.2026.1785372 AbstractBackground: Cor Triatriatum sinister (CTS) is a rare congenital cardiac anomaly caused by a fibromuscular membrane subdividing the left atrium, potentially leading

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Sotatercept in Patients With Eisenmenger Syndrome

Oktay Tutarel, Oliver Miera, Felix BergerDeutsches Herzzentrum der Charité, Freie Universität Berlin and Humboldt-Universität zu Berlin.Germany Pulmonary CirculationPulm Circ 2026; 16: DOI: 10.1002/pul2.70283 AbstractEisenmenger syndrome represents a complex and severe form of pulmonary arterial hypertension (PAH) associated with congenital heart disease. Sotatercept, a first-in-class activin-signaling inhibitor, offers a novel therapeutic approach in the treatment of PAH,

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Case Report: A pediatric case of chronic active Epstein-Barr virus infection complicated by pulmonary arterial hypertension

Meng Zhang, Kai Wang, Xinyi Xu, Wei Ji, Tingliang Liu, Wei Gao, Ying GuoShanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University.China Frontiers in Cardiovascular MedicineFront Cardiovasc Med 2026; 13: DOI: 10.3389/fcvm.2026.1724841 AbstractObjective: To enhance clinicians’ awareness of pulmonary arterial hypertension (PAH) complicating chronic active Epstein-Barr virus infection (CAEBV) in pediatric patients.Method: Clinical data of a

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A Combination Of Vein Of Galen Aneurysmal Malformation And Bovine Aortic Arch In Newborn: A Case Report

Krishna Deo Mandal, Kalpana Subedi, Unnati Amatya, Janak PathakParopakar Maternity and Women’s Hospital. Embassy of India.Nepal Journal of the Nepal Medical AssociationJ Nepal Med Assoc 2025; 63: 347-349DOI: 10.31729/jnma.8987 AbstractVein of Galen aneurysmal malformation is a rare intracranial arteriovenous malformation, coexistence with aortic arch anomalies is even more uncommon, carry high risk of morbidity and mortality

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Liver herniation in congenital diaphragmatic hernia is associated with delayed resolution of pulmonary hypertension

Uthaya Kumaran Kanagaraj, Mimi T.Y. Kuan, Michael Castaldo, Erik Skarsgard, Joseph Y. TingUniversity of British Columbia. University of Alberta.Canada Pediatrics and NeonatologyPediatr Neonatol 2026; DOI: 10.1016/j.pedneo.2025.11.011 AbstractBackground: Severe and persistent pulmonary hypertension (PH) predicts mortality and short-term pulmonary morbidity in infants with congenital diaphragmatic hernia (CDH). Intrathoracic liver herniation (liver-up) is a predictor of survival and increased

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Expanding the phenotypic spectrum of MECOM-associated syndrome: rare variants are associated with syndromic pulmonary arterial hypertension

Carrie L. Welch , Meriel McEntagart, Shahin Moledina, Cara Morgan, Emilia Swietlik, Chao Hou, Lu Qiao, Emily Callejo, Savanna Craib, Damian Smedley, Emilia K. Bijlsma, Patrice Bouvagnet, Nahir Cortes-­Santiago, Tamir Dagan, Jacqueline Eason, Frances Flinter, Aakash Joshi, Jeremie Mortreux, Fadel E. Ruiz, Deborah Shears, Celia Azevedo Soares, Nidhy P. Varghese, Wendy K ChungBoston Children’s Hospital,

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The relationship between muscle strength and oxygenation and activities of daily living in adolescents and young adults with pulmonary arterial hypertension

Jan Dik, Ceyhun Topcuoglu, Naciye Vardar-Yagli, Merve Basol Goksuluk, Ebru Aypar, Dursun Alehan, Melda SaglamHacettepe University. Munzur University. Sakarya University. Turkey Cardiology in the YoungCardiol Young 2026; DOI: 10.1017/S1047951125110895 AbstractPulmonary arterial hypertension leads to dyspnoea, fatigue, and oxygen desaturation, limiting activities of daily living and functional capacity. This study aimed to evaluate the impact of pulmonary

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High altitude pulmonary oedema in the Himalayas: a preventable condition

Tsering Norboo, Keith BallSonam Norboo Memorial Hospital.India PractitionerPractitioner 1988; 232: 557-560DOI: Not Available AbstractHigh altitude pulmonary oedema (HAPO) is an important cause of disability in those visiting the Himalayas. Many visitors and their doctors are apparently unaware of this serious and potentially lethal condition, though it can readily be prevented by ascending slowly and using

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Increased lung vasoreactivity in children from Leadville, Colorado, after recovery from high-altitude pulmonary edema

James W. Fasules, James W. Wiggins, Robert R. WolfeUniversity of Colorado School of Medicine.United States CirculationCirculation 1985; 72: 957-962DOI: 10.1161/01.cir.72.5.957 AbstractCardiac catheterization was performed on seven children after recovery from high-altitude pulmonary edema. All were life-long residents at elevations above 10,000 feet. Three of the seven had developed pulmonary edema without antecedent travel to low altitude

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