Surgical repair of unusual variant of double-outlet right ventricle with discordant atrioventricular connections and superior-inferior ventricles. [PDF]
JTCVS Tech, 2023 Al Kindi H +6 more
europepmc +3 more sources
The independence of the infundibular building blocks in the setting of double-outlet right ventricle. [PDF]
Cardiology in the Young, 2017 It has long been contentious as to whether the presence of bilateral infundibulums, or conuses, is a prerequisite for the diagnosis of double-outlet right ventricle.
Diane E. Spicer +10 more
core +2 more sources
A Quite Rare Association: Levo-Malposition of the Great Arteries with Left Juxtaposition of the Atrial Appendages in “Double Outlet Right Ventricle" [PDF]
Brazilian Journal of Cardiovascular Surgery, 2021 Although many anatomical variations may be encountered in children with double outlet right ventricle, coexistence of levo-malposed great vessels and left juxtaposed atrial appendages is uncommonly observed. This case report underlines the rarity of this
Betül Çınar +4 more
doaj +2 more sources
Visualization of the complex double-outlet right ventricle anatomy using real-time three-dimensional computer graphics. [PDF]
JTCVS Tech, 2023 Omori A, Inuzuka R, Hirata Y.
europepmc +2 more sources
Right Aortic Arch with Isolated Left Subclavian Artery in Association with Double Outlet Right Ventricle and Cor Triatriatum Sinister: Hitherto Unreported Association. [PDF]
Indian J Radiol Imaging, 2023 Bhatia H +3 more
europepmc +3 more sources
Double Outlet Right Ventricle: A Rare Finding in a 15‐Month‐Old Female With Failure to Thrive [PDF]
Clinical Case ReportsDouble outlet right ventricle (DORV) is a rare congenital heart defect where both the aorta and pulmonary artery originate from the right ventricle, often accompanied by additional cardiac anomalies to mitigate circulatory imbalance, though such ...
Bernadette Pedun +4 more
doaj +2 more sources
Holt-oram syndrome associated with double outlet right ventricle: A rare association
Annals of Pediatric Cardiology, 2013 Holt-Oram syndrome is a rare inherited disorder that causes abnormalities of the hands, arms, and the heart. Most commonly, there are defects in the carpal bones of the wrist and in the bones of the thumb along with cardiac defects such as atrial or ...
Bhupinder Singh +3 more
doaj +2 more sources
Annals of Pediatric Cardiology, 2019 A 3-year-old child with a complex variant of double outlet right ventricle achieved a successful biventricular repair after detailed delineation of the intracardiac anatomy on multimodality imaging.
Swati Garekar +10 more
doaj +2 more sources
Annals of Pediatric Cardiology, 2019 An unguarded atrioventricular orifice is an extremely rare congenital anomaly characterized by the absence of the atrioventricular valve in varying proportions.
Anand Subramanian +2 more
doaj +2 more sources
Usefulness of transaortic approach for a complex double-outlet right ventricle. [PDF]
Indian J Thorac Cardiovasc Surg, 2022 Fernandez-Doblas J +4 more
europepmc +3 more sources