Abstract
J wave syndromes are a collection of clinical entities characterized by accentuation of the Ito-mediated J wave, early repolarization and ST segment elevation. Although the risks of sudden cardiac death of these syndromes differ with respect to the magnitude and location of abnormal J wave manifestation and ST segment elevation, they share with a common ionic and cellular mechanism and their responses to heart rate and autonomic influences are similar. The congenital forms of J wave syndromes include early repolarization syndrome, which can be categorized into three subtypes according to J wave location and the risk of arrhythmogenesis, and the Brugada syndrome. J wave syndromes can be acquired in certain pathological conditions with augmentation of J-wave like hypothermia and acute ST segment elevation myocardial infarction. In the chapter, we attempt to summarize current state of knowledge about J-wave syndromes, bridging basic and clinical aspects.
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Lian, J., Kowey, P.R., Yan, GX. (2011). J Wave Syndromes. In: Yan, GX., Kowey, P. (eds) Management of Cardiac Arrhythmias. Contemporary Cardiology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-60761-161-5_21
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