Abstract
Brugada syndrome is a rare autosomal dominant condition characterized by mutations in cardiac sodium channels, which cause specific ECG findings and increase the risk of ventricular fibrillation and sudden cardiac death. Untreated Brugada syndrome has mortality of about 10% per year. The sole effective treatment is placement of an implantable cardiac defibrillator.
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BrugadaDrugs.org. [Online]. [cited 2016 June 14. Available from: http://www.brugadadrugs.org/
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Mankowitz, S. (2018). Brugada Syndrome. In: Mankowitz, S. (eds) Consults in Obstetric Anesthesiology. Springer, Cham. https://doi.org/10.1007/978-3-319-59680-8_25
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DOI: https://doi.org/10.1007/978-3-319-59680-8_25
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