Back

Homozygosity predominantly affects hypertrophic cardiomyopathy minor genes in an Egyptian clinical cohort

26 August 2022 (08:00 - 19:30)
Organised by:
Congress Presentation Part of: Cardiomyopathies Genetics, Epigenetics, ncRNA ESC Professional Premium Access ESC Congress 2022

About the speaker

Photo
Doctor Mona Allouba

Aswan Heart Centre and Research - Magdi Yacoub Foundation, Aswan (Egypt)

6 More presentations in this session

Presentation thumbnail
Phenotypic predictors of pathogenic variants in probands with hypertrophic cardiomyopathy
Doctor D. Ranganathan (Montreal, CA)
Abstract Slides
Presentation thumbnail
Pathogenic variants damage cell compositions and single cell transcription in cardiomyopathies
Doctor D. Reichart (Munich, DE)
Abstract Slides
Presentation thumbnail
LTBP2 mutation may cause mitral valve prolapse
Doctor R. Durst (Jerusalem, IL)
Abstract Slides
Presentation thumbnail
High prevalence of deleterious variants in cardiomyopathy genes in patients with early onset atrial fibrillation
Mr O. Vad (Copenhagen, DK)
Abstract Slides
Presentation thumbnail
A transgenic mouse model mimicking human cardiac amyloidosis
Professor F. Bauer (Le Kremlin-Bicetre, FR) Doctor C. Fauvel (Rouen, FR)
Abstract Slides

Access the full session

Session thumbnail
Cardiomyopathies

The Event

Event poster

ESC Congress 2022

26 August - 29 August 2022

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources