Congenital long QT syndrome

Once considered an extremely rare yet lethal arrhythmogenic peculiarity, congenital long QT syndrome (LQTS) is understood today as a primary cardiac arrhythmia syndrome (cardiac channelopathy) that is both far more common and, overall, much less lethal than previously recognized. Clinically, LQTS is...

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Bibliographic Details
Main Authors: Michael J. Ackerman, Anant Khositseth, David J. Tester, Peter J. Schwartz
Other Authors: Mayo Medical School
Format: Chapter
Published: 2018
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/19452
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Institution: Mahidol University

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