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
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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 |
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2003 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
2023 | 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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Value of 3D echocardiography in the diagnosis of arrhythmogenic right ventricular cardiomyopathy. Eur Heart J Cardiovasc Imaging. 2023 04 24; 24(5):664-677.
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Spatial and transmural properties of the reentrant ventricular tachycardia circuit in arrhythmogenic right ventricular cardiomyopathy: Simultaneous epicardial and endocardial recordings. Heart Rhythm. 2021 06; 18(6):916-925.
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Outcomes of Catheter Ablation in Arrhythmogenic Right Ventricular Cardiomyopathy Without Background Implantable Cardioverter Defibrillator Therapy: A Multicenter International Ventricular Tachycardia Registry. JACC Clin Electrophysiol. 2019 01; 5(1):55-65.
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Genetic and epigenetic regulation of arrhythmogenic cardiomyopathy. Biochim Biophys Acta Mol Basis Dis. 2017 08; 1863(8):2064-2069.
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A Brief Review and Update of the Clinicopathologic Diagnosis of Arrhythmogenic Cardiomyopathy. Arch Pathol Lab Med. 2015 Sep; 139(9):1181-6.
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Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population. Circ Cardiovasc Genet. 2013 Aug; 6(4):327-36.
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Ablation of ventricular arrhythmias in arrhythmogenic right ventricular dysplasia/cardiomyopathy: arrhythmia-free survival after endo-epicardial substrate based mapping and ablation. Circ Arrhythm Electrophysiol. 2011 Aug; 4(4):478-85.
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Characterization of the arrhythmogenic substrate in ischemic and nonischemic cardiomyopathy implications for catheter ablation of hemodynamically unstable ventricular tachycardia. J Am Coll Cardiol. 2010 May 25; 55(21):2355-65.
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MR Imaging of arrhythmogenic right ventricular cardiomyopathy: morphologic findings and interobserver reliability. Cardiology. 2003; 99(3):153-62.