Harvard Catalyst Profiles

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Brugada Syndrome

"Brugada Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.


This graph shows the total number of publications written about "Brugada Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Brugada Syndrome" was a major or minor topic of these publication.
Bar chart showing 65 publications over 17 distinct years, with a maximum of 7 publications in 2013 and 2015 and 2016 and 2018
To see the data from this visualization as text, click here.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.