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Clinical and molecular spectrum of patients with methylmalonic acidemia and homocysteinemia complicated by cardiovascular manifestations

Wanqing Zhao, Yanan Zhang, Yalei Pi, Yuqian Li, Huifeng ZhangSecond Hospital of Hebei Medical University. China Orphanet Journal of Rare DiseaseOrphanet J Rare Dis 2025; DOI: 10.1186/s13023-025-03907-w AbstractBackground: To investigate the clinical characteristics, treatment response, and prognosis of patients with methylmalonic acidemia (MMA) and homocysteinemia complicated by cardiovascular manifestations and to raise awareness regarding MMA and homocysteinemia.Methods: A […]

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Pulmonary Arterial Hypertension Requiring Medication Is Associated With Higher Prevalence of Thrombocytopenia in Pediatric Patients

Tanya Reyna, Catherine Agarwal, Abrar Mamun, Jessica Dae, Yusuf Ozcan, Michael J. Angtuaco, Taha Bat, Erhan AraratUniversity of Texas Southwestern Medical Center. University of Texas at Dallas. University of Arkansas for Medical Sciences.United States Pediatric PulmonologyPediatr Pulmonol 2025; 60: DOI: 10.1002/ppul.71252 AbstractAbstract Not Available CategoryAcquired Patient Factors Associated with Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary

Pulmonary Arterial Hypertension Requiring Medication Is Associated With Higher Prevalence of Thrombocytopenia in Pediatric Patients Read More »

Left Main Bronchus Stenosis Leading to Bronchiectasis and Pulmonary Hypertension- Relieved by Stent Placement

Patrick Stafler, Nili Schamroth, Arnon Elizur, Dario Prais, Eyal Jacobi, Zvi Bar-Sever, Tamir Dagan, Einat Birk, Elchanan BruckheimerSchneider Children’s Medical Center of Israel. Tel Aviv University. Rabin Medical Center. Yitzhak Shamir Medical Center. Israel Pediatric PulmonologyPediatr Pulmonol 2025; 60: DOI: 10.1002/ppul.71251 AbstractAbstract Not Available CategoryClass III. Pulmonary Hypertension Associated with Airway Disease, Apnea or HypoventilationSurgical and

Left Main Bronchus Stenosis Leading to Bronchiectasis and Pulmonary Hypertension- Relieved by Stent Placement Read More »

Utility of inhaled nitric oxide for pulmonary hypertension in cyanotic congenital heart disease: a cohort study with propensity score matching

Xiaofeng Wang, Chenyu Li, Shilin Wang, Zhiyuan Zhu, Qinnan Chen, Ruihuan Shen, Xu WangNational Center for Cardiovascular Disease and Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College. Fuwai Yunnan Hospital, Chinese Academy of Medical Sciences amd Affiliated Cardiovascular Hospital of Kunming Medical University. Sir Run Run Shaw Hospital and Zhejiang University

Utility of inhaled nitric oxide for pulmonary hypertension in cyanotic congenital heart disease: a cohort study with propensity score matching Read More »

Factors Influencing Prolonged Hospital Stay in Surgically Treated Children and Adolescents with Left-to-Right Shunt Congenital Heart Disease: Evidence From a Hospital in Southern China

Liudan Huang, Yuhua Zhang, Shaobo JiangMeizhou People’s Hospital and Meizhou Academy of Medical Sciences.China Therapeutics and Clinical Risk ManagementTher Clin Risk Manag 2025; DOI: 10.2147/TCRM.S533273 AbstractBackground: Congenital heart disease(CHD) is a congenital malformation caused by abnormal development of the heart and large blood vessels, and left-to-right shunt CHD is a relatively common type. Surgical treatment has the

Factors Influencing Prolonged Hospital Stay in Surgically Treated Children and Adolescents with Left-to-Right Shunt Congenital Heart Disease: Evidence From a Hospital in Southern China Read More »

Life-saving stepwise management of pulmonary hypertension in an infant with Down syndrome presenting with a large patent ductus arteriosus and giant hepatic arteriovenous malformation

Emine Gulsah Torun, Nevin Özdemiroglu, Velihan Cayhan, Ibrahim EceAnkara Bilkent City Hospital. Gaziantep City Hospital. Turkey Cardiology in the Young Cardiol Young 2025; DOI: 10.1017/S1047951125101662 AbstractWe report a rare case of a 3-month-old male infant with Down syndrome, severe pulmonary arterial hypertension (a large patent ductus arteriosus, an atrial septal defect, and a giant hepatic arteriovenous

Life-saving stepwise management of pulmonary hypertension in an infant with Down syndrome presenting with a large patent ductus arteriosus and giant hepatic arteriovenous malformation Read More »

Cardio-Respiratory Complications in Adult Monozygotic Twins With Myhre Syndrome

Hyoungjun Sim, Forrest Wilke, Emily Hamburger, Charlie J. Sang 3rd, Clara HildebrandtUniversity of North Carolina. United States American Journal of Medical Genetics Part C Seminars in GeneticsAm J Med Genet C Semin Med Genet 2025; DOI: 10.1002/ajmg.c.32150 AbstractMyhre syndrome is a rare connective tissue disorder characterized by skeletal, cardiopulmonary, dermatologic, neurocognitive changes, and a predisposition to

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Echocardiographic correlation of right ventricular-Pulmonary artery coupling to exercise tolerance in congenital heart disease-associated pulmonary hypertension

Anudya Kartika Ratri, Ovin Nada Saputri, David Nugraha, Ricardo Adrian Nugraha, Alisia Yuana Putri, Meity Ardiana, Budi Susetyo Pikir, I. Gde Rurus SuryawanUniversitas Airlangga. Dr. Soetomo General Academic Hospital. Indonesia Annals of Pediatric CardiologyAnn Pediatr Cardiol 2025; 18: 26-32DOI: 10.4103/apc.apc_230_24 AbstractBackground: Pulmonary arterial hypertension (PAH) is a chronic, progressive disease affecting the pulmonary vasculature, with a high

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SUL-150 Limits Vascular Remodeling and Ventricular Failure in Pulmonary Arterial Hypertension

Lysanne M. Jorna, Dalibor Nakládal, Johannes N. van Heuveln, Diederik E. van der Feen, Quint A. J. Hagdorn, Guido P. L. Bossers, Annemieke van Oosten, Michel Weij, Ludmila Tkáciková, Sona Tkáciková, Robert H. Henning, Martin C. Harmsen, Rolf M. F. Berger, Guido KrenningUniversity Medical Center Groningen, University of Groningen. Comenius University Bratislava. University of Heidelberg.

SUL-150 Limits Vascular Remodeling and Ventricular Failure in Pulmonary Arterial Hypertension Read More »

State of the Art: Complex Peripheral Pulmonary Artery Reconstruction Techniques

Elisabeth Martin, Michael Ma, Frank HanleyStanford University School of Medicine and Lucile Packard Children’s Hospital.United States Seminars in Thoracic and Cardiovascular Surgery Pediatric Cardiac Surgery AnnualSemin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2025; 28: 101-106DOI: 10.1053/j.pcsu.2025.03.002 AbstractOver the last several years, we developed and improved our surgical approach to patients requiring pulmonary artery reconstruction in

State of the Art: Complex Peripheral Pulmonary Artery Reconstruction Techniques Read More »

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