"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.
Descriptor ID |
D053840
|
MeSH Number(s) |
C14.280.067.322 C14.280.123.250 C16.320.100
|
Concept/Terms |
Brugada Syndrome- Brugada Syndrome
- Sudden Unexplained Death Syndrome
- Brugada Syndrome 1
- Brugada Syndrome 1s
- Sudden Unexplained Nocturnal Death Syndrome
- Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome
- Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
|
Below are MeSH descriptors whose meaning is more general than "Brugada Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Brugada Syndrome".
This graph shows the total number of publications written about "Brugada Syndrome" by people in this website by year, and whether "Brugada Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2009 | 3 | 0 | 3 |
2010 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
2016 | 2 | 0 | 2 |
2017 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2021 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Brugada Syndrome" by people in Profiles.
-
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Circulation. 2023 03 07; 147(10):824-840.
-
A novel familial SCN5A exon 20 deletion is associated with a heterogeneous phenotype. J Electrocardiol. 2021 May-Jun; 66:131-135.
-
iPSC-Cardiomyocyte Models of Brugada Syndrome-Achievements, Challenges and Future Perspectives. Int J Mol Sci. 2021 Mar 10; 22(6).
-
Reply to letter "A fatal adverse event upon adenotonsillectomy in a child. Are Brugada syndrome and propofol real accomplices?" Cardiol Young. 2020 09; 30(9):1370-1371.
-
Post-operative Brugada electrocardiographic pattern, polymorphic ventricular tachycardia, and sudden death in a child after administration of propofol anaesthesia. Cardiol Young. 2020 May; 30(5):724-727.
-
The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 02; 21(2):398-408.
-
Utility of 12-lead and signal-averaged Holter electrocardiograms after pilsicainide provocation for risk stratification in Brugada syndrome. Heart Vessels. 2017 Sep; 32(9):1151-1159.
-
The utility of T-wave alternans during the morning in the summer for the risk stratification of patients with Brugada syndrome. Heart Vessels. 2017 Mar; 32(3):341-351.
-
Characterization of the epicardial substrate for catheter ablation of Brugada syndrome. Heart Rhythm. 2016 11; 13(11):2151-2158.
-
Insight into specific pro-arrhythmic triggers in Brugada and early repolarization syndromes: results of long-term follow-up. Heart Vessels. 2016 Dec; 31(12):2035-2044.