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