Article

Utility of genetic screening for the prediction of severe arrhythmic outcomes in mitral valve prolapse

2026-06-24

Abstract excerpt

<h4>Background</h4> Cardiomyopathy and channelopathy (CC) gene variants have been linked to sudden cardiac arrest (SCA) or death (SCD) in small, selected pedigree or post-mortem studies of arrhythmic mitral valve prolapse (MVP). However, the utility of clinical whole exome sequencing (WES) panels as a risk stratification tool in unselected MVP samples is unknown. <h4>Objectives</h4> The goal of the study was to...

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Literature Corpus work: e1a1896e-9e40-516d-b25a-2e49d3818aa0
DOI: 10.64898/2026.06.22.26356215

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