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Brugada Syndrome is a rare but serious autosomal dominant cardiac disorder, primarily affecting Asian males. It is characterized by an increased risk of ventricular tachyarrhythmias and sudden cardiac death (SCD).
A hallmark of Brugada Syndrome is a distinct ECG pattern, which includes:
These findings are often more pronounced in fever, electrolyte imbalances, or certain medications.
The primary preventive strategy is the implantation of an implantable cardioverter-defibrillator (ICD) for high-risk patients.
Feature | Description |
---|---|
Genetics | Autosomal dominant |
Most Affected | Asian males |
ECG Findings | Pseudo-RBBB, ST elevation (V1-V3) |
Complications | Ventricular tachyarrhythmias, SCD |
Treatment | Implantable cardioverter-defibrillator (ICD) |