A Rare Case: Brugada Syndrome


YILDIRIM M. K. , Orhan S., KARABACAK P. , Ceylan B. G. , Eroglu F., KARABACAK M.

JOURNAL OF THE TURKISH SOCIETY OF INTENSIVE CARE-TURK YOGUN BAKM DERNEGI DERGISI, cilt.15, ss.77-80, 2017 (ESCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 15 Konu: 2
  • Basım Tarihi: 2017
  • Doi Numarası: 10.4274/tybdd.92408
  • Dergi Adı: JOURNAL OF THE TURKISH SOCIETY OF INTENSIVE CARE-TURK YOGUN BAKM DERNEGI DERGISI
  • Sayfa Sayıları: ss.77-80

Özet

Brugada syndrome is an electrocardiography (ECG) abnormality with a high incidence of sudden death in patients. It is characterized by typical ECG abnormalities such as ST elevation in precordial leads. Brugada syndrome is due to a mutation in the cardiac sodium channel genes. This syndrome can lead to a dangerous rhythm disorders such as ventricular fibrillation. Herein we presented a case who did not have any cardiac disorder, however had ventricular tachycardia and type 1 Brugada ECG pattern seen with cardiac arrest.