A Congenital Deadly Association: Dilated Cardiomyopathy and Long QT Syndrome

A Congenital Deadly Association: Dilated Cardiomyopathy and Long QT Syndrome

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Long QT syndrome is one of the most feared entities in hospitalized patients due to the potential risk for ventricular tachycardia and sudden death. Association between channelopathies and congenital cardiomyopathy is a new entity that has been studied recently. We report an interesting case of this...

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Bibliographic Details
Main Authors: Neiberg de Alcantara Lima, Antonio Thomaz de Andrade, Stela M V Sampaio, Mark Loehrke
Format: Article
Language:English
Published: Linceu Editorial 2020-10-01
Series:Journal of Cardiac Arrhythmias
Subjects:
Long QT Syndrome
Cardiomyopathies
Genetic Diseases
Ventricular Tachycardia
Channelopathies
Online Access:https://jca.emnuvens.com.br/jca/article/view/3426

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