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
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| 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 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 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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Genetic inactivation of ?-catenin is salubrious, whereas its activation is deleterious in desmoplakin cardiomyopathy. Cardiovasc Res. 2023 12 30; 119(17):2712-2728.
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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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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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TMEM43-S358L mutation enhances NF-?B-TGF? signal cascade in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Protein Cell. 2019 02; 10(2):104-119.
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Cardiac sarcoidosis presenting as arrhythmogenic right ventricular cardiomyopathy/dysplasia with ventricular aneurysms: a case report. Cardiovasc Pathol. 2018 Mar - Apr; 33:1-5.
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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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Fibroblasts and the extracellular matrix in right ventricular disease. Cardiovasc Res. 2017 Oct 01; 113(12):1453-1464.
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Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation. J Am Heart Assoc. 2015 Jan 23; 4(1):e001526.