OasisLMS

Arrhythmogenic cardiomyopathy (ACM) is a rare, inherited cardiac disorder associated with ventricular arrhythmias, fibrofatty myocardial replacement, and sudden cardiac death (SCD). Mutations in the plakophilin-2 (PKP2) gene are the most common cause of ACM. Currently, there are no diseasemodifying therapies for PKP2-ACM; standard care focuses on arrhythmia control and SCD prevention through antiarrhythmics, ICDs, and ablation, without addressing the underlying cause.

Moderator
Andrew Krahn

Speakers
Dominic Abrams
David Duncker
Fasial Merchant
Mina Chung
Harikrishna Tandri
Hawkins Gay
Mehak Dhande