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

28 August 2022 (16:15 - 17:00)
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Congress Presentation Part of: Cardiomyopathies Genetics, Epigenetics, ncRNA ESC Professional Premium Access ESC Congress 2022

About the speaker

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Doctor Mona Allouba

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

6 More presentations in this session

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

The Event

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ESC Congress 2022

28 August 2022 16:15 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources