Arrhythmogenic Right Ventricular Dysplasia
"Arrhythmogenic Right Ventricular Dysplasia" 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.
A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias.
| Descriptor ID |
D019571
|
| MeSH Number(s) |
C14.240.400.145 C14.280.238.028 C14.280.400.145 C16.131.240.400.145
|
| Concept/Terms |
Arrhythmogenic Right Ventricular Dysplasia- Arrhythmogenic Right Ventricular Dysplasia
- Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia
- Arrhythmogenic Right Ventricular Cardiomyopathy Dysplasia
- Ventricular Dysplasia, Right, Arrhythmogenic
- ARVD-C
- Right Ventricular Dysplasia, Arrhythmogenic
- Arrhythmogenic Right Ventricular Cardiomyopathy
- Arrhythmogenic Right Ventricular Dysplasia-Cardiomyopathy
|
Below are MeSH descriptors whose meaning is more general than "Arrhythmogenic Right Ventricular Dysplasia".
Below are MeSH descriptors whose meaning is more specific than "Arrhythmogenic Right Ventricular Dysplasia".
This graph shows the total number of publications written about "Arrhythmogenic Right Ventricular Dysplasia" by people in this website by year, and whether "Arrhythmogenic Right Ventricular Dysplasia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 |
| 2004 | 0 | 1 | 1 |
| 2006 | 2 | 0 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2020 | 1 | 0 | 1 |
| 2022 | 2 | 0 | 2 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Arrhythmogenic Right Ventricular Dysplasia" by people in Profiles.
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Desmoplakin Cardiomyopathy in Pediatric Patients: A Distinct, Underrecognized Cohort of Arrhythmogenic Cardiomyopathy. Circ Arrhythm Electrophysiol. 2024 Nov; 17(11):e013114.
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The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure. Cardiovasc Res. 2022 05 06; 118(6):1466-1478.
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Progressive Reduction in Right Ventricular Contractile Function Attributable to Altered Actin Expression in an Aging Mouse Model of Arrhythmogenic Cardiomyopathy. Circulation. 2022 05 24; 145(21):1609-1624.
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Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility. Sci Rep. 2020 12 10; 10(1):21622.
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RNA sequencing-based transcriptome profiling of cardiac tissue implicates novel putative disease mechanisms in FLNC-associated arrhythmogenic cardiomyopathy. Int J Cardiol. 2020 03 01; 302:124-130.
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Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation. Mol Genet Genomic Med. 2019 06; 7(6):e593.
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Distinct Cellular Basis for Early Cardiac Arrhythmias, the Cardinal Manifestation of Arrhythmogenic Cardiomyopathy, and the Skin Phenotype of Cardiocutaneous Syndromes. Circ Res. 2017 Dec 08; 121(12):1346-1359.
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A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome. Am J Med Genet A. 2013 Feb; 161A(2):371-6.
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Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy. J Am Coll Cardiol. 2010 Feb 09; 55(6):587-97.
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Animal models of arrhythmogenic cardiomyopathy. Dis Model Mech. 2009 Nov-Dec; 2(11-12):563-70.