Brugada syndrome: Case report
Author(s) -
V. Bisenić,
Saša Hinić,
Mirjana Krotin,
Branislav Milovanović,
J. Saric,
Goran Milašinović
Publication year - 2012
Publication title -
srpski arhiv za celokupno lekarstvo
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.135
H-Index - 17
eISSN - 2406-0895
pISSN - 0370-8179
DOI - 10.2298/sarh1202084b
Subject(s) - medicine , brugada syndrome , palpitations , cardiology , sudden cardiac death , st elevation , sudden death , ventricular fibrillation , electrocardiography , acute coronary syndrome , myocardial infarction
Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment elevation and J point elevation of at least 2 mm in at least two of the right precordial ECG leads (V1-3) and ventricular arrhythmias, syncope, and sudden death. Risk stratifications of patients with Brugada electrocardiogram are being strongly debated.
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