Results 11 to 20 of about 3,071 (219)

Quadricuspid Aortic Valve: Report of Two Cases and Brief Review [PDF]

open access: yesCase Reports in Cardiology, 2019
Quadricuspid aortic valve (QAV) is a rare congenital cardiac defect characterized by the presence of four aortic valve leaflets of equal or varying sizes. Even rarer is its clinical presentation with aortic stenosis. Diagnosis of QAV could be challenging
Oreoluwa Oladiran   +3 more
doaj   +4 more sources

Type A Quadricuspid Aortic Valve Infective Endocarditis Complicated by Multiple Aortocardiac Fistulae: Case Report and Brief Literature Review [PDF]

open access: yesCase Reports in Cardiology, 2017
Aortocardiac fistulae (ACF) are exceptionally due to infective endocarditis; they are usually congenital, posttraumatic, or complicate aortic dissection.
Amine Ghalem   +5 more
doaj   +3 more sources

Quadricuspid Aortic Valve With Severe Aortic Regurgitation. [PDF]

open access: goldClin Case Rep
ABSTRACT Whenever a quadricuspid aortic valve (QAV) was present, it was historically only identified during open heart surgery. However, recent advances in transthoracic echocardiography have made it possible to detect QAV preoperatively. Further evaluation using transesophageal echocardiography or computed tomography before open surgery may help guide
Minatoya T   +6 more
europepmc   +4 more sources

Transcatheter Aortic Valve Replacement in Patients With Quadricuspid Aortic Valve: A Case Series and Systematic Review. [PDF]

open access: goldCardiol Res Pract
Background: Quadricuspid aortic valve (QAV) is a rare congenital cardiac anomaly associated with symptomatic aortic regurgitation (AR) or aortic stenosis (AS). Transcatheter aortic valve replacement (TAVR) for QAV remains uncertain. Methods: We retrospectively reviewed prospectively collected data from patients with QAV undergoing TAVR in our center ...
Sheng W   +5 more
europepmc   +4 more sources

Transthoracic echocardiography and its limitations in the diagnosis of congenital supernumerary aortic valve in a Thoroughbred

open access: yesVeterinary Medicine and Science, 2023
Aortic valve malformation is a common congenital abnormality reported in human medicine. The malformation is characterised by an increased or decreased number of cusps. Anatomical variations of the aortic valve that have been documented in humans include
Valentina Vitale   +2 more
doaj   +2 more sources

Quadricuspid Aortic Valve With Guarded Left Coronary Artery Ostium in an Infant With Myocardial Infarction [PDF]

open access: gold, 2022
Anatomical variations of the aortic valve include unicuspid, bicuspid, and quadricuspid. The bicuspid aortic valve is most common and affects 1%-2% of the general population. QAV is generally an isolated malformation, and adults most commonly present
Kimball, Thomas Richard   +3 more
core   +4 more sources

Type F congenital quadricuspid aortic valve: A very rare case diagnosed by 3-dimenional transoesophageal echocardiography [PDF]

open access: hybrid, 2014
Congenital quadricuspid aortic valve (QAV) is a rare cardiac anomaly. Several different anatomical variations of a quadricuspid aortic valve have been described.
Cooke JC   +17 more
core   +4 more sources

Quadricuspid Aortic Valve: Out of the Shadows, into the Light [PDF]

open access: yesDiagnostics
We present the case of a 63-year-old man with severe aortic valve regurgitation and left-ventricular dysfunction. The patient was scheduled for elective surgery.
Dmitri Panfilov   +2 more
doaj   +2 more sources

Quadricuspid Aortic Valve: Imaging, Diagnosis, and Prognosis [PDF]

open access: yesTexas Heart Institute Journal
Quadricuspid aortic valve is a rare congenital cardiac anomaly with an incidence of 0.008% to 0.043%. Its clinical course varies depending on cusp anatomy, function, and associated cardiac malformations.
Mohammad Alomari, MD   +5 more
doaj   +2 more sources

Quadricuspid aortic valve repair: Results of a phenotype-based approachCentral MessagePerspective [PDF]

open access: yesJTCVS Techniques
Objective: Quadricuspid aortic valve (QAV) anatomy is a rare congenital anomaly. Patients develop relevant aortic regurgitation (AR), commonly between the fourth and sixth decades of life.
Karen B. Abeln, MD   +3 more
doaj   +2 more sources

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