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Phenotypic and prognostic differences in carriers with loss-of-function type missense SCN5A variants

30 August 2026 (09:15 - 10:00)
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Congress Presentation Part of: Inherited arrhythmia syndromes: mechanisms, genotype–phenotype correlations, and risk stratification Ion Channel Disorders ESC2026 Premium Access ESC Congress 2026 European Society of Cardiology

About the speaker

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Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)

6 More presentations in this session

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NLRP3 inflammasome related signaling contributing to pathogenesis of Brugada Syndrome
Miss C. Yan (Mannheim, DE)
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Computational modeling of timothy syndrome using a human induced pluripotent stem cell-derived ventricular cardiomyocyte model with improved Ca²⁺current dynamics
Doctor A. Trancuccio (Pavia, IT)
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Assessment of ventricular conduction in Brugada patients by morphological characterization of QRS complexes
Doctor S. Romagnoli (Zaragoza, ES)
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Variant-specific mechanisms of KCNJ2 dysfunction and their genotype–phenotype correlations in Andersen–Tawil syndrome
Doctor K. Kato (Otsu, JP)
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Buccal cell proteomics reveals myocardial ATP1B1 deficiency in brugada syndrome
Mr L. Mcguire (London, GB)
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Inherited arrhythmia syndromes: mechanisms, genotype–phenotype correlations, and risk stratification

The Event

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ESC Congress 2026

30 August 2026 09:15 CET
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