Summaries for thematic area 2: Cardiomyopathies

This thematic area covers the inherited arrhythmia syndromes in which the heart is structurally abnormal. The heart muscle can be too thick or too thin or functions abnormal due to discrete structural abnormalities. These diseases are caused by variants in genes encoding for proteins that play a role in many different processes in cardiac cells. Diseases included are Arrhythmogenic cardiomyopathy, Hypertrophic cardiomyopathy, Dilated cardiomyopathy, Restrictive cardiomyopathy, and Unclassified cardiomyopathy.

Original work

Electrocardiogram analysis in Anderson-Fabry disease: a valuable tool for progressive phenotypic expression tracking (Parisi)
Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity? (Van der Crabben)
Longitudinal prediction of ventricular arrhythmic risk in ARVC (Te Riele)
Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator (Protonotarios)
Programmed Ventricular Stimulation as an Additional Primary Prevention Risk Stratification Tool in ARVC (Gasperetti)
Syncope in hypertrophic cardiomyopathy (part II): An expert consensus statement on the diagnosis and management (Limongelli)
Natural history of MYH7-related dilated cardiomyopathy (de Frutos)

Guidelines