A Rare Case: Brugada Syndrome

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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, sa.2, ss.77-80, 2017 (ESCI, Scopus, TRDizin)

• Yayın Türü: Makale / Tam Makale
• Cilt numarası: 15 Sayı: 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
• Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
• Sayfa Sayıları: ss.77-80
• Süleyman Demirel Üniversitesi Adresli: Evet

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.