Identification of ultra-rare variants in dilated cardiomyopathy: insights into LMNA pathogenesis and prognostic significance

29 August 2025 (07:00 - 18:00)

Organised by:

Sign in to view the resources

Sign in for access options

About the speaker

Doctor Takeshi Kitai

National Cerebral & Cardiovascular Center, Suita (Japan)

5 More presentations in this session

Presentation thumbnail

The impact of desmosomal mutations on clinical features in arrhythmogenic cardiomyopathy: towards tailored arrhythmic risk stratification

Doctor M. Martini (Padova, IT)

Abstract Slides

Presentation thumbnail

Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies for gene discovery

Ms D. Kramarenko (Amsterdam, NL)

Abstract Slides

Presentation thumbnail

Predictors of the identification of clinically relevant genetic variants in dilated cardiomyopathy in a sample of the brazilian population

Mr L. Cedro (Sao Paulo, BR)

Abstract Slides

Presentation thumbnail

Gain-of-function vs. loss-of-function effects of DES variants on cardiodesminopathy phenotypes

Mr M. Urtis (Pavia, IT)

Abstract Slides

Presentation thumbnail

The clinical spectrum of TTN variants in families affected by dilated cardiomyopathy: evidence for a pre-clinical phenotype

Doctor F. Goldie (Glasgow, GB)

Abstract Slides

Access the full session

Session thumbnail

Improved understanding of the genetic background of cardiomyopathy

The Event

Event poster

ESC Congress 2025

29 August - 1 September 2025

You may be interested in

Congress Presentation

Genotype-driven prognostication in dilated cardiomyopathy

Congress Presentation

Genetic determinants of disease severity in idiopathic dilated cardiomyopathy

Congress Presentation

LMNA variants distribution and their impact on the cardiac phenotypic spectrum

ESC 365 is supported by

novartis

Explore sponsored resources

ESC 365 is supported by

novartis

Explore sponsored resources