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References OMIM Gene GeneReviews HGMD HGNC
last update : 21-11-2016
Symbol BRGS5
Location 19q13.12
Name Brugada syndrome 5
Corresponding gene SCN1B
Other symbol(s) BRGDA5
Main clinical features
  • syncope, sudden cardiac death, or epilepsy, palpitations and dizziness and complete left bundle branch block on electrocardiogram (ECG)
  • characterized by a distinct ST-segment elevation in the right precordial leads of the electrocardiogram and, clinically, by an increased risk of cardiac arrhythmia and sudden death
  • Genetic determination autosomal dominant
    Function/system disorder cardiovascular
    Type disease