ESC Professional Premium Access

Reinterpretation of variant of unknown significance in the clinical setting of inherited cardiac conditions

Topic: Genetic Aspects of Arrhythmias

Congress Session

About the speaker

Doctor Valeria Novelli

IRCCS Monzino Cardiology Center, Milan (Italy)
0 follower

4 more presentations in this session

Clinical role of genetic testing for overlapping between Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy

Speaker: Assistant Professor J. Jeong (Seoul, KR)

Thumbnail

Genetic variation rs6795970 of the SCN10A gene is associated with PR interval in young population of Republic of Moldova

Speaker: Mrs C. Butovscaia (Chisinau, MD)

Thumbnail

Functional analysis of novel SCN5A mutations related to Brugada syndrome

Speaker: Mrs H. Namgoong (Seoul, KR)

Thumbnail

Risk stratification of sudden cardiac death in subjects with asymptomatic ventricular preexcitation: diagnostic value of non-invasive and invasive methods

Speaker: Doctor L. Pilon Kaial (Rosario, AR)

Thumbnail

Access the full session

Inherited cardiac disorders

Speakers: Doctor V. Novelli, Assistant Professor J. Jeong, Mrs C. Butovscaia, Mrs H. Namgoong, Doctor L. Pilon Kaial
Thumbnail

About the event

Image

ESC Congress 2022

26 August - 29 August 2022

Sessions Presentations

This platform is supported by

logo Novo Nordisk