ESC Professional Premium Access

Calmodulinopathy is a common cause of critical cardiac phenotypes in fetus and infancy

Congress Presentation

About the speaker

Doctor Megumi Fukuyama

Shiga University of Medical Science, Otsu (Japan)
0 follower

4 more presentations in this session

SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome

Speaker: Professor V. Probst (Nantes, FR)


Natural History of Patients with Typical and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia

Speaker: Doctor A. Trancuccio (Pavia, IT)


Longitudinal validation of the phospholamban (PLN) p.Arg14del risk model

Speaker: Miss M. Van Der Heide (Amsterdam, NL)


Efficacy and safety of the ICD in patients with catecholaminergic polymorphic ventricular tachycardia

Speaker: Assistant Professor A. Mazzanti (Pavia, IT)


Access the full session

Emerging role of genetic testing for ventricular arrhythmia management

Speakers: Doctor M. Fukuyama, Professor V. Probst, Doctor A. Trancuccio, Miss M. Van Der Heide, Assistant Professor A. Mazzanti

About the event


ESC Congress 2022

26 August - 29 August 2022

Sessions Presentations

ESC 365 is supported by

logo Novo Nordisk
logo Bristol Myers Squibb