Volume 8, Issue 11, Pages (November 2011)

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Volume 8, Issue 11, Pages 1686-1695 (November 2011) Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations Barbara Bauce, MD, PhD, Alessandra Rampazzo, PhD, Cristina Basso, MD, PhD, Elisa Mazzotti, MD, PhD, Ilaria Rigato, MD, PhD, Alexandros Steriotis, MD, PhD, Giorgia Beffagna, PhD, Alessandra Lorenzon, PhD, Marzia De Bortoli, PhD, Kalliopi Pilichou, PhD, Martina Perazzolo Marra, MD, PhD, Francesco Corbetti, MD, Luciano Daliento, MD, Sabino Iliceto, MD, Domenico Corrado, MD, PhD, Gaetano Thiene, MD, Andrea Nava, MD Heart Rhythm Volume 8, Issue 11, Pages 1686-1695 (November 2011) DOI: 10.1016/j.hrthm.2011.06.026 Copyright © 2011 Heart Rhythm Society Terms and Conditions

Figure 1 A: 12-lead ECG of a 10-year-old family member (DSP mutation carrier) who did not fulfill the 1994 and recently modified diagnostic criteria. The ECG trace is normal. B: SAECG of the same patient, with no late potentials at 40 filter settings. C: CMR of the same patient with T1 sequence showing no fat infiltration. D: CMR of the same patient showing LE on the LV wall (arrows). Heart Rhythm 2011 8, 1686-1695DOI: (10.1016/j.hrthm.2011.06.026) Copyright © 2011 Heart Rhythm Society Terms and Conditions

Figure 2 Event-free survival rates in terms of major events according to the underlying genetic background. Heart Rhythm 2011 8, 1686-1695DOI: (10.1016/j.hrthm.2011.06.026) Copyright © 2011 Heart Rhythm Society Terms and Conditions