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The Brugada syndrome described in 1992 is a genetically conditioned canalopathy responsible for the development of ventricular fibrillation and sudden cardiac death. Burgada syndrome and Brugada phenotype are differed, which are characterized by the presence of a typical ECG pattern: blockade of the right ventriculonector leg and elevation of the ST segment in the right thoracic leads. Unlike the syndrome, Brugada phenotype is transient. ECG diagnosis in various clinical situations can be difficult. This article presents a clinical case of newly diagnosed Brugada syndrome in an elderly patient with distrust to an acute coronary syndrome.

BRUGADA-TYPE ECG IN THE PATIENT OF 75 YEARS OLDS