Cardiac conduction defects

Cardiac conduction defects

Authors

  • Giulia Guerri MAGI’s Lab, Rovereto (TN), Italy
  • Geraldo Krasi MAGI Balkans, Tirana, Albania
  • Vincenza Precone MAGI Euregio, Bolzano, Italy
  • Stefano Paolacci MAGI'S LAB
  • Pietro Chiurazzi Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, Rome, Italy; UOC Genetica Medica, Fondazione Policlinico Universitario "A. Gemelli", Rome Italy
  • Luca Arrigoni Section of Cardiovascular Diseases, Department of Clinical and Surgical Specialities, Radiological Sciences and Public Health, University and Spedali Civili Hospital of Brescia, Italy
  • Bernardo Cortese Cardiac Department, San Carlo Clinic, Milan, Italy
  • Astrit Dautaj MAGI Balkans, Tirana, Albania
  • Matteo Bertelli MAGI Euregio, Bolzano, Italy

Keywords:

Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, long QT syndrome, short QT syndrome, Wolff-Parkinson-White syndrome, familial atrial fibrillation

Abstract

Defects in cardiac electric impulse formation or conduction can lead to an irregular beat (arrhythmia) that can cause sudden death without any apparent cause or after stress. In the following sections, we describe the genetic disorders associated with primary cardiac conduction defects, primarily caused by mutations in ion channel genes. Primary indicates that these disorders are not caused by drugs and are not secondary to other disorders like cardiomyopathies (described in the next section).

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Published

30-09-2019

How to Cite

1.
Guerri G, Krasi G, Precone V, Paolacci S, Chiurazzi P, Arrigoni L, et al. Cardiac conduction defects. Acta Biomed [Internet]. 2019 Sep. 30 [cited 2024 Aug. 17];90(10-S):20-9. Available from: https://mattioli1885journals.com/index.php/actabiomedica/article/view/8751