Results 41 to 50 of about 836,225 (279)

Physiological and clinical consequences of relief of right ventricular outflow tract obstruction late after repair of congenital heart defects. [PDF]

, 2006
BACKGROUND: Right ventricular outflow tract obstruction (RVOTO) is a common problem after repair of congenital heart disease. Percutaneous pulmonary valve implantation (PPVI) can treat this condition without consequent pulmonary regurgitation or ...
Sridharan, S, Schievano, S, Coats, L, Jones, R, Mist, B, Taylor, AM, Deanfield, JE, Bonhoeffer, P, Derrick, G, Khambadkone, S, Pellerin, D   +10 more
core  

Valved stents for transapical pulmonary valve replacement [PDF]

, 2009
OBJECTIVES: Pulmonary valve insufficiency remains a leading cause for reoperations in congenital cardiac surgery. The current percutaneous approach is limited by the size of the access vessel and variable right ventricular outflow tract morphology.
von Segesser, L.K., Hurni, Michel, Hurni, M., von Segesser, Ludwig K., Huber, Christoph H, Huber, Christoph H., Tsang, Victor, Tsang, V., von Segesser, Ludwig K, Huber, C.H.   +9 more
core   +1 more source

Systematic Cardiac Phenotyping of Patients With Copy Number Variants in the 15q11.2 Breakpoint 1 to Breakpoint 2 Region: A Retrospective Cohort Study From Nine Pediatric Cardiac Centers

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright, Maria B. Padua, Lindsey R. Helvaty, Kim L. McBride, Gabrielle Geddes, Vidu Garg, Seema R. Lalani, Stephanie Burns Wechsler, Jennelle C. Hodge, Benjamin J. Landis, Stephanie M. Ware   +10 more
wiley   +1 more source

Ultrasound-guided serratus anterior plane block for transapical transcatheter aortic valve implantation

Journal of Cardiothoracic Surgery, 2023
Background Reducing postoperative pain due to the thoracotomy incisions in patients undergoing transapical transcatheter aortic valve implantation remains a challenge.
Ling Peng, Meng Ding, Wei Wei
doaj   +1 more source

Pulmonary valvulotomy in a fetus with pulmonary atresia with intact ventricular septum : first experience in Turkey [PDF]

, 2012
The mortality and morbidity of children with pulmonary atresia with intact ventricular septum (PA/IVS) is closely related with right ventricle hypoplasia and its consequent hemodynamics.
Polat, Tugcin Bora, Danısman, N.
core  

Longitudinal Echocardiographic Surveillance of Aortic Dilation in a Phenotype‐Enriched Turner Syndrome Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Turner syndrome (TS) is associated with thoracic aortopathy and increased risk for aortic dissection, yet the natural history of aortic dilation is not well understood. We performed a retrospective longitudinal study of individuals with TS who participated in the TS Society of the United States Healthy Heart Project between 2003 and 2023 ...
Dylan Doerner, Matthew R. Johnson, Sara Mansoorshahi, Rakesh Kathiresan, Katelyn Abel, Jonathan G. You, Emilio Quezada, Siddharth K. Prakash   +7 more
wiley   +1 more source

Early post-operative benefits of a pulmonary valve-sparing strategy during Fallot repair

International Journal of Cardiology Congenital Heart Disease, 2022
Background: Patients undergoing complete repair of tetralogy of Fallot generally have an excellent prognosis. Unfortunately, pulmonary valve reconstruction with a transannular patch is generally required.
Taher Touré, François Roubertie, Tiphaine Bridier, Hélène Foulgoc, Jean-Benoît Thambo, Alexandre Ouattara, Nadir Tafer   +6 more
doaj   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source

Clinical Case of Surgical Correction of Infective Endocarditis of the Pulmonary Valve Associated with Infundibular Stenosis in an Adult

Український журнал серцево-судинної хірургії
Background. Congenital heart defects, if not surgically corrected in a timely manner, are a predictor for the development of infective endocarditis, with the likelihood of its occurrence increasing with patient age. Aim.
Roman Yo. Lekan, Volodymyr St. Moroz, Taras Vo. Romaniuk, Ivan Ro. Lekan, Lyudmyla Va. Balaban   +4 more
doaj   +1 more source

A Rare Cardiac Anomaly in Absent Pulmonary Valve Syndrome with Tetralogy of Fallot [PDF]

, 2018
Heart failure and cardiomegaly are observed in patients with absent pulmonary valve syndrome with tetralogy of Fallot (TOF), unlike in those with TOF alone. Additional cardiac anomalies can also be seen in these patients, although not frequently.
Emine Hekim Yılmaz, Ahmet Çelebi, Gökmen Akgün, Selma Oktay Ergin, Taliha Öner   +4 more
core   +1 more source