- Emergency
- Prenatal information.
- Congenital heart defects.
- Atrial septal defect (ASD).
- Atrioventricular septal defect (AVSD).
- Ventricular septal defect (VSD).
- Aortopulmonary window.
- Aortic arch anomalies.
- Coarctation of the aorta.
- Interrupted aortic arch.
- Persistent ductus arteriosus (PDA).
- Cor triatriatrum.
- Ebstein’s anomaly.
- Pulmonary stenosis.
- Fallot’s tetralogy.
- Coronary artery anomalies.
- D-transposition of the great arteries (d-TGA).
- Aortic stenosis (AS).
- Total anomalous pulmonary venous connection (TAPVC).
- Pulmonary atresia with intact ventricular septum (PA + IVS).
- Double Outlet Right Ventricle (DORV).
- Truncus Arteriosus (TA).
- Hypoplastic left heart syndrome (HLHS).
- Univentricular heart (UVH).
- Treatment principles.
- Heart transplantation in infancy and childhood.
- Children's ward.
Ebstein’s anomaly
Ebstein's anomaly is characterised by displacement of the tricuspid valve into the right ventricle. The original boundary of the atrium persists as a valveless ring. There is usually more or less severe tricuspid insufficiency. The operation, performed with the heart-lung machine, consists of tightening the “atrialised“ right ventricle, which moves the tricuspid valve into the correct anatomical plane. In this condition, an artificial prosthetic valve can be implanted as a last resort.
- Ebstein's anomaly