Brugada Syndrome (BrS)

Brugada syndrome is an inherited cardiac channelopathy that increases the risk of dangerous ventricular arrhythmias and sudden cardiac arrest. It is characterized by a distinctive ECG pattern and can present with fainting, palpitations, or no symptoms at all. Because onset can occur at any age and the condition may be silent until a serious event, genetic testing can aid in confirming the diagnosis and guiding management.