HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

Michael J. Ackerman(Mayo Clinic in Florida), Silvia G. Priori(Fondazione Salvatore Maugeri), Stephan Willems(University Medical Center Hamburg-Eppendorf), Charles I. Berul(Children's National), Ramón Brugada(University of Girona), Hugh Calkins(Johns Hopkins University), A. John Camm(St George's, University of London), Patrick T. Ellinor(Texas Cardiac Arrhythmia), Michael H. Gollob(University of Ottawa), Robert M. Hamilton(Hospital for Sick Children), Ray E. Hershberger(University of Miami), Daniel P. Judge(Université Paris Cité), Hervé Le Marec(Institut du Thorax), William J. McKenna(University College London), Eric Schulze‐Bahr(University Hospital Münster), Christopher Semsarian(University of Sydney), Jeffrey A. Towbin(Cincinnati Children's Hospital Medical Center), Hugh Watkins(John Radcliffe Hospital), Arthur A.M. Wilde(University of Amsterdam), Christian Wolpert(Klinikum Ludwigsburg), Douglas P. Zipes(Indiana University – Purdue University Indianapolis)
EP Europace
August 1, 2011
Cited by 900Open Access
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Abstract

This international consensus statement provides the state of genetic testing for the channelopathies and cardiomyopathies. It summarizes the opinion of the international writing group members based on their own experience and on a general review of the literature with respect to the use and role of genetic testing for these potentially heritable cardiac conditions. This document focuses primarily on the state of genetic testing for the 13 distinct entities detailed and the relative diagnostic, prognostic, and therapeutic impact of the genetic test result for each entity. It does not focus on the therapeutic management of the various channelopathies and cardiomyopathies. Treatment/ management issues are only discussed for those diseases (i.e., LQTS, HCM, DCM + CCD, RCM) in which the genetic test result could potentially influence treatment considerations.


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