ABC | Volume 113, Nº2, August 2019

Review Article Lamounier Júnior et al. Genetic and dilated cardiomyopathy Arq Bras Cardiol. 2019; 113(2):274-281 Study Association This article is part of the thesis of master submitted by Filipe Ferrari, from Graduate Program in Cardiology and Cardiovascular Sciences, Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre. Ethics approval and consent to participate This article does not contain any studies with human participants or animals performed by any of the authors. Figure 1 – Cardiac magnetic resonance imaging showing extensive and diffuse area of mesocardial fibrosis. Figure 2 – Index case heredogram showing involvement in first, second and third degree relatives. AF: atrial fibrillation. I.1 Sudden death at 36 yearsold III.3 Suddendeath at46 yearsold III.4 Sudden deathat 45 years old V.1 Age: 10 years V.2 Age:8 years IV.2 E1–/+ Dilated cardiomyopathy+AF Diagnosisat29 years old Heart transplantation: 31 yearsold III.7 Suddendeathat 49 yearsold III.8 Suddendeathat 48 yearsold III.11 Suddendeath at 39 yearsold II.2 Dilated cardiomyopathy II.3 Dilated cardiomyopathy III.2 Dilated cardiomyopathy II.1 II.4 III.1 IV.1 P IV.3 III.5 III.6 III.9 III.10 I.2 Suddendeath at32 yearsold 279