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Ebstein's anomaly is a congenital heart defect in which the septal and posterior leaflets of the tricuspid valve are displaced downwards towards the apex of the right ventricle of the heart. [1] EA has great anatomical heterogeneity that generates a wide spectrum of clinical features at presentation and is complicated by the fact that the ...
English: 12-lead ECG of a woman with Ebstein's anomaly (a congenital heart defect in which the opening of the tricuspid valve is displaced towards the apex of the right ventricle of the heart, resulting in a large right atrium). The ECG shows signs of right atrial enlargement, best seen in V1.
Ebstein also published works in regards to medical illness of prominent Germans in history, such as Martin Luther and Arthur Schopenhauer. [4] His name was attached to the eponymous Ebstein's anomaly (a rare congenital heart defect) [10] and Pel–Ebstein fever (a remittent fever associated with Hodgkin's disease). [11]
The majority of cases can be diagnosed prenatally during a routine anomaly scan. If evidence of a congenital heart disease is found, the diagnosis can be confirmed by a foetal echocardiogram . If it is not diagnosed prenatally, it may be diagnosed shortly after birth with physical examination, which would reveal cyanosis and murmur.
Ebstein's anomaly is an abnormality of the tricuspid valve, and its presence can lead to tricuspid valve regurgitation. [16] [18] A bicuspid aortic valve [16] is an aortic valve with only 2 cusps as opposed to the normal 3. It is present in about 0.5% to 2% of the general population and causes increased calcification due to higher turbulent ...
Ebstein's anomaly [31] – about 50% of individuals with Ebstein anomaly have an associated shunt between the right and left atria, either an atrial septal defect or a patent foramen ovale. [32] Fetal alcohol syndrome – about one in four patients with fetal alcohol syndrome has either an ASD or a ventricular septal defect. [33]
Those affected by arrhythmogenic cardiomyopathy may not have any symptoms at all despite having significant abnormalities in the structure of their hearts. [6] If symptoms do occur, the initial presentation is often due to abnormal heart rhythms (arrhythmias) which in arrhythmogenic cardiomyopathy may take the form of palpitations, or blackouts. [7]
746.2 Ebstein's anomaly; 746.3 Congenital stenosis of aortic valve; 746.4 Congenital insufficiency of aortic valve; 746.5 Congenital mitral stenosis; 746.6 Congenital mitral insufficiency; 746.7 Hypoplastic left heart syndrome; 746.8 Other specified congenital anomalies of heart. 746.81 Subaortic stenosis congenital; 746.82 Cor triatriatum