by Dr. Peter McCullough, Global Research:

Brugada syndrome is a rare but potentially life-threatening inherited disease that predisposes patients to fatal cardiac arrhythmias. The syndrome is characterized by the ECG findings of a right bundle branch block and ST-segment elevations in the right precordial leads (V1-V3). More than 400 mutations in the cardiac SCN5A gene have been identified in people with Brugada syndrome, which is characterized by risk of cardiac arrest, particularly in the setting of fever.