"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 |
| 2009 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2014 | 3 | 0 | 3 |
| 2016 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
| 2024 | 1 | 1 | 2 |
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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 09 03; 18(35):24060-24075.
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Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci. Eur Heart J. 2024 Jul 09; 45(26):2320-2332.
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GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death. EBioMedicine. 2020 Jul; 57:102843.
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Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry. Circ Genom Precis Med. 2020 08; 13(4):e002797.
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Loperamide Mimicking Brugada Pattern. Methodist Debakey Cardiovasc J. 2018 Oct-Dec; 14(4):e1-e3.
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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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Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome. Sci Rep. 2014 Oct 23; 4:6733.
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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.
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Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome. Sci Rep. 2014 Jan 27; 4:3850.
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Diagnosis and management of pediatric brugada syndrome: a survey of pediatric electrophysiologists. Pacing Clin Electrophysiol. 2014 May; 37(5):638-42.