"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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 2 | 0 | 2 |
| 2011 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Brugada Syndrome" by people in Profiles.
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Multimodal Mapping of Electrical and Mechanical Latency of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocyte Layers. ACS Nano. 2024 Sep 03; 18(35):24060-24075.
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Potential Diagnostic Role for a Combined Postmortem DNA and RNA Sequencing for Brugada Syndrome. Circ Genom Precis Med. 2023 12; 16(6):e004251.
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Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Circulation. 2023 03 07; 147(10):824-840.
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Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands. Circ Genom Precis Med. 2021 10; 14(5):e003222.
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Lacosamide induced Brugada I morphology in the setting of septicemia: A case report. Medicine (Baltimore). 2021 May 07; 100(18):e25577.
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Loperamide Mimicking Brugada Pattern. Methodist Debakey Cardiovasc J. 2018 Oct-Dec; 14(4):e1-e3.
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Progressive and Reversible Conduction Disease With Checkpoint Inhibitors. Can J Cardiol. 2017 10; 33(10):1335.e13-1335.e15.
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Electrocardiographic abnormalities in elite high school athletes: comparison to adolescent hypertrophic cardiomyopathy. Br J Sports Med. 2016 Jan; 50(2):105-10.
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Suicide left ventricle due to conduction disturbance following transcatheter aortic valve replacement and reversal with restoration of sinus rhythm: is there life after death? J Invasive Cardiol. 2015 Jun; 27(6):E107-9.
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Heart rate-corrected QT interval is an independent predictor of all-cause and cardiovascular mortality in individuals with type 2 diabetes: the Diabetes Heart Study. Diabetes Care. 2014 May; 37(5):1454-61.