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New phenotypic association for SMAD6 gene: its role in the development of cardiac conduction disorders and pulmonary arterial hypertension/hereditary haemorrhagic telangiectasia.

29 August 2025 (07:00 - 18:00)
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Congress Presentation Part of: Mechanisms of arrhythmias Genetic Aspects of Arrhythmias ESC Professional Premium Access ESC Congress 2025 European Society of Cardiology

About the speaker

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Doctor Almudena Amor Salamanca

Health in Code, Cardiology Department, Madrid (Spain)

7 More presentations in this session

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Piezo1-Mediated TGF-beta2 autocrine loop promotes atrial fibrosis and fibrillation under pressure overload
Doctor H. Wu (Xi'an, CN)
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Genetic factors in risk stratification of concealed long QT patients with no history of beta-blocker use
Doctor A. Savelev (Lund, SE)
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Elucidation of the pathogenesis in long QT syndrome caused by a CALM2 variant, p.D134H, using knock-in mouse model
Doctor S. Ohno (Suita, JP)
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Therapeutic effect of selective serotonin reuptake inhibitors to gain-of-function KCND3 variant identified in a patient with early repolarization and refractory epilepsy.
Doctor T. Byambajav (Suita, JP)
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New genetic risk factor for serious cardiac events in Andersen-Tawil Syndrome - p.Arg71Gln variant in BAG3.
Ms M. Krych (Warsaw, PL)
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Access the full session

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Mechanisms of arrhythmias

The Event

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ESC Congress 2025

29 August - 1 September 2025
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ESC 365 is supported by

novartis Explore sponsored resources