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Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease- associated large deletion in the SCN5A gene  Anders Krogh Broendberg,

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Presentation on theme: "Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease- associated large deletion in the SCN5A gene  Anders Krogh Broendberg,"— Presentation transcript:

1 Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease- associated large deletion in the SCN5A gene  Anders Krogh Broendberg, MD, Lisbeth Noerum Pedersen, MSc, PhD, Jens Cosedis Nielsen, MD, DMSc, PhD, Henrik Kjaerulf Jensen, MD, DMSc, PhD  HeartRhythm Case Reports  Volume 2, Issue 3, Pages (May 2016) DOI: /j.hrcr Copyright © 2016 Heart Rhythm Society Terms and Conditions

2 Figure 1 Family pedigree. Index patient is marked with an arrow.
HeartRhythm Case Reports 2016 2, DOI: ( /j.hrcr ) Copyright © 2016 Heart Rhythm Society Terms and Conditions

3 Figure 2 A: A 12-lead electrocardiogram (ECG) from the index patient with type 1 pattern diagnostic for Brugada syndrome. B: Implantable cardioverter-defibrillator (ICD) interrogation in the index patient, with ventricular fibrillation eliciting appropriate and effective ICD therapy. C: A 12-lead ECG from the son of the index patient. HeartRhythm Case Reports 2016 2, DOI: ( /j.hrcr ) Copyright © 2016 Heart Rhythm Society Terms and Conditions

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