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Short QT phenotype in a family with genetic variants in the KCNH2 and SLC4A3 genes - The role of prediction tools, whole exome sequencing and genetic cascade screening

Congress Presentation

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Doctor Boldizsar Kovacs

University of Michigan Hospital, Ann Arbor (United States of America)
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7 more presentations in this session

Ethnical differences in patients with brugada syndrome and arrhythmic events: new insights from sabrus

Speaker: Doctor A. Milman (Tel Hashomer, IL)


Genotype-phenotype correlations in patients with arrhythmogenic cardiomyopathy: results from next generation sequencing in a large multicenter cohort

Speaker: Assistant Professor A. Saguner (Zurich, CH)


Safety of general anesthesia in brugada syndrome

Speaker: Doctor G. Ciconte (San Donato Milanese, IT)


Risk of progression to malignant ventricular arrhythmia's in carriers of the cardiomyopathy causing (PLN) p.Arg14del mutation

Speaker: Mr T. Verstraelen (Amsterdam, NL)


Prognostic implications of non-sustained ventricular tachycardia morphology in high-risk patients with hypertrophic cardiomyopathy

Speaker: Doctor C. Adduci (Rome, IT)


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Moderated ePosters 8: channelopathies & cardiomyopathies

Speakers: Doctor B. Kovacs, Doctor A. Milman, Assistant Professor A. Saguner, Doctor G. Ciconte, Mr T. Verstraelen...

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EHRA 2019

17 March - 19 March 2019

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