Population
Patients with nonischemic dilated cardiomyopathy (DCM) and their family members
Design
Review
Authors
Loading...
May guide DCM evaluation and family screening; leaves open prospective validation of arrhythmia risk stratification.
Genetic evaluation in nonischemic dilated cardiomyopathy aids in refining disease subtypes, predicting prognosis (especially arrhythmia risk), and enabling early intervention through cascade testing in family members.
McNally et al. (2017) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: