Brugada Syndrome
- PMID: 30137852
- Bookshelf ID: NBK519568
Brugada Syndrome
Excerpt
Brugada syndrome is a genetic disease that predisposes patients to fatal cardiac arrhythmias. It is named after Josep and Pedro Brugada who first described it in 1992. 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).
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References
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- Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol. 1992 Nov 15;20(6):1391-6. - PubMed
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- Littmann L, Monroe MH, Kerns WP, Svenson RH, Gallagher JJ. Brugada syndrome and "Brugada sign": clinical spectrum with a guide for the clinician. Am Heart J. 2003 May;145(5):768-78. - PubMed
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