Results 71 to 80 of about 1,136,669 (183)

Exploring Health‐Related Quality of Life in Children With Pulmonary Hypertension

Pulmonary Circulation, Volume 15, Issue 4, October 2025.
ABSTRACT Pulmonary hypertension (PH) in children requires complex medical management. Health‐related quality of life (HRQoL) remains understudied in this population. During an 8‐month period children and parents attending PH outpatient appointments completed the generic PedsQL (measuring physical, emotional, social, and school functioning).
Jo Wray, Sadia Quyam, Holly Clisby, Vicky Kelly, Shahin Moledina   +4 more
wiley   +1 more source

Prenatal Diagnosis of Horseshoe Lung: A Report of Three Cases and Review of the Literature

Prenatal Diagnosis, Volume 45, Issue 8, Page 1027-1038, July 2025.
ABSTRACT Objective Horseshoe lung is a rare congenital malformation in which the lungs are fused by a parenchymal isthmus. The current literature is very limited regarding cases of prenatal diagnosis and their outcome. Method We retrospectively examined three cases of fetuses with horseshoe lung diagnosed antenatally in our center from 2015 to 2024 ...
Benjamin Birene, Paul Maurice, Catherine Garel, Blandine Prevost, Yohan Soreze, Maud Chabaud, Jean‐Marie Jouannic   +6 more
wiley   +1 more source

Emergency Transmediastinal Pneumonectomy for Scimitar Syndrome

, 2010
Repair of scimitar syndrome presenting in infancy involves either tunneling or reimplantation of the anomalous vein to the left atrium and may be fraught with serious complications such as thrombosis and secondary pulmonary infarction necessitating ...
John K. Papagiannis, George V. Kirvassilis, George E. Sarris, Panagiotis G. Sfyridis, Irene D. Lytrivi   +4 more
core   +1 more source

Surgical management of scimitar syndrome: An alternative approach [PDF]

, 2003
Objective: The scimitar syndrome is a congenital anomaly that consists in part of total or partial anomalous venous drainage of the right lung to the inferior vena cava.
Uhlig, Paul N., Ruzmetov, Mark, Minnich, Douglas J., Brown, John W., Edwards, Christopher A., Turrentine, Mark W., Vijay, Palaniswamy, Fiore, Andrew C.   +7 more
core   +1 more source

Breathing With Half a Pulmonary Circuit: Three Cases of Unilateral Pulmonary Artery Agenesis

Respirology Case Reports, Volume 13, Issue 7, July 2025.
We present three cases of unilateral pulmonary artery atresia (UPAA) with varying clinical presentations and radiological findings, highlighting the diverse manifestations of this rare condition and discussing the current understanding of its pathophysiology, diagnostic approaches, and management strategies. ABSTRACT Unilateral pulmonary artery atresia
Vignesh Kumar Kathiresan, Benjamin Earnest Williams, V. S. Aswith Chowdary Jonnalagadda   +2 more
wiley   +1 more source

Scimitar syndrome: a European Congenital Heart Surgeons Association (ECHSA) multicentric study

, 2010
BACKGROUND: Scimitar syndrome is a rare congenital heart disease. To evaluate the surgical results, we embarked on the European Congenital Heart Surgeons Association (ECHSA) multicentric study. METHODS AND RESULTS: From January 1997 to December 2007, we
Marco Pozzi, Mark Hazekamp, Sairanen, H, Donato, R. di, Meyns, B, Stellin, G, Heikki Sairanen, Urban, Andreas, Fragata, J, Andreas Urban, Vida, V.L., Padalino, M A, Pretre, R., Sertaç Çiçek, Tlaskal, Tomas, Bohdan Maruszewski, Roberto Di Donato, Metras, Dominique, Pozzi, M, Vida, Vladimiro L, METRAS D, Ciçek, Sertaç, Hazekamp, M, Sarris, G., SCHREIBER C, Giovanna Boccuzzo, Ciçek, S, Schreiber, Christian, Vida, V L, Prêtre, René, Bart Meyns, Rubay, J, Hazekamp, Mark, FRAGATA J, Thiene, G., Berggren, Hakan, Metras, D., DI DONATO R, Pozzi, M., Meyns, Bart, Carlo, D, Padalino, M, Di Donato, R, Pozzi, Marco, Tlaskal, T., Urban, A., HRASKA V, Thiene, G, Pretre, R, Thierry Carrel, Dominique Metras, POZZI M, Gaetano Thiene, Fragata, J., Schreiber, C., Maruszewski, Bohdan, SAIRANEN H, Sarris, George, Vladimiro L. Vida, Padalino, M.A., Di Carlo, D, Tarja, Erjon, Di Carlo, Duccio, Sairanen, H., Crupi, G., MARUSZEWSKI B, BERGGREN H, Hraska, Viktor, Erjon Tarja, Crupi, Giancarlo, VIDA VL, CRUPI G, TLASKAL T, Thiene, Gaetano, Boccuzzo, Giovanna, Maruszewski, B, Duccio Di Carlo, Giovanni Stellin, Carlo, D. di, Cicek, S., Jean Rubay, Stellin, Giovanni, Boccuzzo, G., Stellin, G., HAZEKAMP M, George Sarris, Maruszewski, B., Meyns, B., Metras, D, TARJA E, Tlaskal, T, Crupi, G, Hazekamp, M., Berggren, H, RUBAY J, CARREL T, URBAN A, Christian Schreiber, Carrel, T, Padalino, Massimo A, Carrel, Thierry, Rubay, J., Urban, A, CICEK S, SARRIS G, Berggren, H., PADALINO MA, Viktor Hraska, Hakan Berggren, Hraska, V., Boccuzzo, G, Rene Pretre, Tarja, E., Vida, V, MEYNS B, Carrel, T., Schreiber, C, José Fragata, Tomas Tlaskal, Rubay, Jean, Vida, Vladimiro L., Massimo A. Padalino, Di Donato, Roberto, Sairanen, Heikki, Sarris, G, PRETRE R, Fragata, José, Giancarlo Crupi, Donato, R, Tarja, E, Hraska, V, DI CARLO D   +131 more
core   +1 more source

Robotic Congenital Cardiac Surgery Practice Worldwide: A Systematic Review

Journal of Cardiac Surgery, Volume 2025, Issue 1, 2025.
Background: With the increasing adoption of robotic technology in adult cardiac surgery patients, improved surgeon experience and wider utilization have been reported. However, interpreting trends in robotic congenital surgery is more challenging.
Madonna E. Lee, Andrea Amabile, Irbaz Hameed, James Antonios, Ahmed K. Awad, Alexandria Brackett, Markus Krane, Peter J. Gruber, Arnar Geirsson, Tomás A. Salerno   +9 more
wiley   +1 more source

Fetal Presentation of MYRF‐Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis

Prenatal Diagnosis, Volume 44, Issue 13, Page 1647-1658, December 2024.
ABSTRACT Purpose MYRF‐related cardiac‐urogenital syndrome (MYRF‐CUGS) is a rare condition associated with heterozygous MYRF variants. The description of MYRF‐CUGS phenotype is mostly based on postnatal cases and 36 affected individuals have been published so far.
Maud Favier, Elise Brischoux‐Boucher, Louise C. Pyle, Nicolas Mottet, Marion Auber‐Lenoir, Julie Cattin, Eric Dahlen, Christelle Cabrol, Francine Arbez‐Gindre, Tania Attié‐Bitach, Odile Boute, Louise Devisme, Detlef Trost, Aicha Boughalem, David Chitayat, Lev Prasov, Odelia Chorin, Annick Rein‐Rothschild, Eran Kassif, Tal Weissbach, Laura Godfrey Hendon, Margaret P. Adam, Chloé Quelin, Sylvie Jaillard, Laura Mary, Sietse M. Aukema, Malou Heijligers, Christine de Die‐Smulders, Sander Stegmann, Lauren Badalato, Adi Ben‐Yehuda, Claire Beneteau, Pierre‐Louis Forey, Paul Kuentz, Juliette Piard   +34 more
wiley   +1 more source

Copy number variations: The potential association genetic cause in severe cardiovascular diseases with unknown aetiology

Journal of Cellular and Molecular Medicine, Volume 28, Issue 12, June 2024.
Abstract Cardiovascular diseases (CVDs) are the leading cause of mortality worldwide. While both genetic and environmental factors significantly contribute to the pathogenesis of CVDs, recent advancements in genetic technology have further emphasized the significance of genetic factors in CVDs.
Niloofar Naderi, MohammadHossein MozafaryBazargany, Majid Maleki, Samira Kalayinia   +3 more
wiley   +1 more source

MDCT findings of Scimitar syndrome in an elderly patient

, 2015
Scimitar syndrome is a rare congenital vascular anomaly characterized by abnormal venous drainage of the right lung to the inferior vena.
GEZER, NACİYE SİNEM, UÇAN, EYÜP SABRİ, ALTAY, CANAN, BAŞARA AKIN, IŞIL, BALCI, PINAR   +4 more
core   +1 more source