Recognizing rare cardiac diseases by electrocardiogram

作者：Grimm W^*; Grimm A; Grimm K; Efimova E

来源：Internist, 2018, 59(6): 618-629.

DOI：10.1007/s00108-018-0400-y

• Brugada syndrome
• Long QT syndrome
• Wolff-Parkinson-White syndrome
• Tachycardia
• ventricular
• repetitive monomorphic
• Arrhythmogenic right ventricular cardiomyopathy

A number of rare cardiac diseases can be recognized by electrocardiogram (ECG). This article illustrates the clinical importance of ECG as a key diagnostic tool to detect Wolff-Parkinson-White syndrome and channelopathies, which are frequently diagnosed late after one or more affected family members have become victims of sudden cardiac death. These channelopathies include long QT syndrome, short QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. In addition, typical ECG findings are frequently present in patients with idiopathic ventricular tachycardia, arrhythmogenic right ventricular dysplasia, digitalis intoxication, hyperkalemia, acute cor pulmonale due to pulmonary embolism, as well as severe left ventricular hypertrophy as in hypertrophic cardiomyopathy.

• 出版日期2018-6