Archives of the
Turkish Society of Cardiology
Review

Brugada Syndrome: 30 Years of Scientific Adventure

1.

Division of Cardiovascular Diseases, Department of Cardiology, Brussel, Belgium

Archives of the Turkish Society of Cardiology 2022; 50: 452-458
DOI: 10.5543/tkda.2022.22444
Read: 881 Downloads: 212 Published: 19 July 2022

Thirty years ago, a distinct new clinical-electrocardiographic syndrome was described, now known as Brugada syndrome (BrS). Typical for this syndrome is EKG with ST elevation in the right precordial leads. The clinical presentation of the disease is highly variable: Patients may remain completely asymptomatic, but may also develop episodes of syncope, atrial fibrillation (AF), sick sinus syndrome (SSS), conduction disturbances, asystole, and ventricular fibrillation (VF). The disease is caused by mutations in the genes responsible for the action potential of the heart cells. The most frequently involved gene is the SCN5A which controls the structure and function of the cardiac sodium channel. Describing this new syndrome has had very positive implications in all fields of medicine.

Cite this article as: Brugada P. Brugada syndrome: 30 years of scientific adventure. Turk Kardiyol Dern Ars. 2022;50(6):452-458.

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ISSN 1016-5169 EISSN 1308-4488