Back

Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

29 August 2020 (08:30 - 08:30)
Organised by:
Congress Presentation Part of: Risk of Sudden Cardiac Death in Patient with Ion Channel Disorders Genetic Aspects of Arrhythmias ESC Premium Access ESC Congress 2020

About the speaker

Photo
Ms Manon Baudic

Institute of Thorax, Nantes (France)

5 More presentations in this session

Presentation thumbnail
ICD implantation and device therapy: Fabry vs hypertrophic cardiomyopathy
Doctor R. Vijapurapu (Stoke-on-Trent, GB)
Abstract Slides
Presentation thumbnail
Long-term efficacy and safety of hydroquinidine in patients with Brugada syndrome
Doctor F. Angelini (Turin, IT)
Abstract Slides
Presentation thumbnail
Splice site mutation of LMNA causes severe dilated cardiomyopathy via strong dominant reduction of total lamin expression
Doctor K. Kato (Otsu, JP)
Abstract Slides
Presentation thumbnail
Role of an extensive diagnostic work-up in the detection of concealed cardiomyopathies in athletes with premature ventricular complexes and implications for sports' eligibility assessment
Doctor P. Compagnucci (Ancona, IT)
Abstract Slides
Presentation thumbnail
KCNQ1 V141M and Short QT Syndrome: Are we dealing with a different entity?
Doctor G. Garcia Ordonez (Guadalajara, MX)
Abstract Slides

Access the full session

Session thumbnail
Risk of Sudden Cardiac Death in Patient with Ion Channel Disorders

The Event

Event poster

ESC Congress 2020

29 August 2020 08:30 CET
You may be interested in
thumbnail
Congress Presentation
Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation
27 August 2022
thumbnail
Congress Presentation
FOXK1 regulates wnt signaling to promote cardiac development
21 May 2023
thumbnail
Congress Presentation
Pathogenic mechanism of DSG2-F531C mutation caused arrhythmogenic right ventricular cardiomyopathy
3 September 2019
thumbnail
Congress Presentation
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population
31 August 2019

ESC 365 is supported by

novartis Explore sponsored resources
novo-nordisk Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources
novo-nordisk Explore sponsored resources