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References OMIM Gene GeneReviews HGMD HGNC
last update : 21-11-2016
Symbol BRGS9
Location 1p13.2
Name Brugada syndrome 9
Corresponding gene KCND3
Other symbol(s) BRGDA9
Main clinical features
  • is characterized by ST segment elevation in the right precordial electrocardiogram leads (so-called type 1 ECG) and a high incidence of sudden death in patients with structurally normal hearts
  • the syndrome typically manifests during adulthood, with a mean age of sudden death of 41 +/- 15 years, but also occurs in infants and children
  • Genetic determination autosomal dominant
    Function/system disorder cardiovascular
    Type disease