An Autopsic Examination Case of Diagnosed Brugada Syndrome

Brugada syndrome is a cardiac disorder characterized by typical ECG alterations, and it is associated with a high risk for sudden cardiac death, affecting young subjects with structurally normal hearts. The prevalence of this disorder is still uncertain, presenting marked geographical differences. The syndrome has a genetic basis, and several mutations have been identified in genes encoding subunits of cardiac sodium, potassium, and calcium channels, as well as in genes involved in the trafficking or regulation of these channels. We experienced an autopsy case of the sudden death by diagnosed Brugada syndrome. We present the case report and autopsic findings.