Results 71 to 80 of about 24,054 (264)

Coronary Artery Fistula with Double Outlet Right Ventricle: a Case Report [PDF]

open access: yesJournal of Tehran University Heart Center, 2007
The majority of coronary artery fistulas (CAFs) are congenital. The anomaly accounts for 0.4% of congenital heart defects and approximately 50% of pediatric coronary vasculature anomalies.
Yaser Jenab   +4 more
doaj   +1 more source

Williams Syndrome and Neonatal Cardiac Surgery for Congenital Single Ventricle

open access: yesJACC: Case Reports, 2020
Williams syndrome (WS) is an arteriopathic derangement associated with supravalvular aortic stenosis and branch pulmonary stenosis. We describe double-outlet right ventricle with mitral atresia and aortic arch hypoplasia in an infant with WS.
Taylor E. Katt, MD   +5 more
doaj   +1 more source

Development and Morphology of the Ventricular Outflow Tracts. [PDF]

open access: yes, 2016
It is customary, at the current time, to consider many, if not most, of the lesions involving the ventricular outflow tract in terms of conotruncal malformations.
Anderson, RH   +4 more
core   +2 more sources

Prenatal detection and outcome of major heart defects in a country with universal screening

open access: yesUltrasound in Obstetrics &Gynecology, EarlyView.
ABSTRACT Objective To evaluate the Danish prenatal screening program for major fetal congenital heart defects (mCHD), focusing on incidence, detection rates (DRs), pregnancy outcomes and postnatal mortality. Methods This was a 5‐year nationwide cohort study conducted from January 2018 to December 2022 in Denmark.
C. Vedel   +15 more
wiley   +1 more source

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

open access: yesBMC Pregnancy and Childbirth, 2017
Background To investigate the differences in cardiovascular disease, extracardiac anomalies and outcomes between fetuses with levocardia and dextrocardia.
Xiaofang Wang   +8 more
doaj   +1 more source

Prognostic value of fetal growth and prenatal functional echocardiography in tetralogy of FALLOT

open access: yesActa Obstetricia et Gynecologica Scandinavica, EarlyView.
First demonstration that fetal growth and pulmonary peak velocity at third trimester are independent predictors of postnatal outcome in Tetralogy of Fallot. This may enhance the accuracy of prenatal counseling and facilitate more individualized planning for delivery and neonatal care. Abstract Introduction Tetralogy of Fallot (ToF) shows variability in
Laura Nogué   +17 more
wiley   +1 more source

Double-Outlet Right Ventricular Malformation in a Two-Year-Old Aberdeen Angus Cow

open access: yesAnimals
A 2-year-old Aberdeen Angus cow was presented with lethargy and decreased appetite at the VA-MD College of Veterinary Medicine Large Animal Teaching Hospital.
Baker White   +5 more
doaj   +1 more source

In Vitro Hemocompatibility of the BiVACOR Total Artificial Heart in Continuous and Pulsatile Flow

open access: yesArtificial Organs, EarlyView.
BiVACOR's total artificial heart generates remarkably similar hemocompatibility when operated with a pulse or during continuous flow. Under both conditions, hemolysis and von Willebrand Factor multimers were similar to a commercial reference device after 6 h in vitro evaluation.
Antony P. McNamee   +6 more
wiley   +1 more source

Results of Hemodynamic Correction in Patients with Double Outlet Right Ventricle

open access: yesУкраїнський журнал серцево-судинної хірургії, 2019
Aim. To analyze results of hemodynamic correction in surgical treatment of double outlet right ventricle (DORV). Маterials and methods. For the period from January 1996 to September 2017, 31 (6.03 % of total number of patients with DORV) patients ...
Kh. K. Abralov   +5 more
doaj   +1 more source

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

open access: yesClinical Genetics, EarlyView.
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson   +22 more
wiley   +1 more source

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