Results 61 to 70 of about 439,883 (208)
Understanding atrioventricular septal defect: Anatomoechocardiographic correlation-10
Papillary muscles (asterisk) joined to the right ventricular free wall. The arrow points to the ventricular septal defect. Abbreviations as before.Copyright information:Taken from "Understanding atrioventricular septal defect: Anatomoechocardiographic ...
Luis Muñoz-Castellanos (39502) +3 more
core +1 more source
Operation for partial atrioventricular septal defect: a forty-year review [PDF]
Background: We describe the long-term outcome of repair of partial atrioventricular septal defect by determining the rates of survival, reoperation, and occurrence of left atrioventricular valve regurgitation, left atrioventricular valve stenosis, left ...
Spotts, Bruce E. +6 more
core +1 more source
Reverse offsetting of atrioventricular valves: A case report of a rare finding
We describe a unique case in a 23 year old male with reverse offsetting of the atrioventricular valves in which the attachment of the anterior mitral leaflet to the septum was closer to the apex as compared to the septal leaflet of the tricuspid valve ...
Ashok Garg +3 more
doaj +1 more source
Smartphone heart monitors in pediatric CIEDs: A pilot study. Smartphone heart monitors did not induce EMI in children with CIEDs, enabling reliable heart rate measurement and accurate identification of ventricular non‐captures. ABSTRACT Background Portable heart monitors enable on‐demand electrocardiogram (ECG) recordings and enhance symptom‐rhythm ...
Chun‐Lok Ho +3 more
wiley +1 more source
Familial secundum atrial septal defect with dysrhythmia associated with web neck
Most cases of atrial septal defect occur sporadically, but a few families have the defect as a genetic abnormality. A family having familial type secundum atrial septal defect with dysrhythmia associated with web neck is reported.
Zübeyir Kiliç +4 more
doaj
Robotic surgery for atrial septal defect closure in a case of Kabuki syndrome
Summary– Kabuki syndrome is a rare congenital malformation syndrome characterized by mental retardation, skeletal deformities, auditory dysfunction, cardiac defects, and distinctive facial appearance. Although complex cardiovascular malformations present
Burak Onan +3 more
doaj +1 more source
Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development
Congenital heart disease (CHD) is the most common defect in live births. The role of cyclin‐dependent kinase (CDK13) in cardiogenesis and CHD was studied using a transgenic mouse model (Cdk13tm1b) carrying deletion of exons 3 and 4, causing loss of function.
Qazi Waheed‐Ullah +8 more
wiley +1 more source
The Evolving Landscape of CHD Genetics: A Contemporary Guide to Genetic Testing and Management
ABSTRACT Congenital heart disease (CHD) is the most common birth defect, affecting an estimated 9.4/1000 infants globally. The genetics of CHD is complex, with most cases thought to have multifactorial aetiology, implicating both genetic and environmental factors.
Bridget R. O'Malley +3 more
wiley +1 more source
Creation of ventricular septal defects on the beating heart in a new pig model [PDF]
Background/ Aims: So far, surgical and interventional therapies for muscular ventricular septal defects ( mVSDs) beyond the moderator band have had their limitations. Thus, alternative therapeutic strategies should be developed.
Hinterseer, M. +7 more
core +1 more source

