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 |
|---|
| 2001 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 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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Abnormal termination of Ca2+ release is a common defect of RyR2 mutations associated with cardiomyopathies. Circ Res. 2012 Mar 30; 110(7):968-77.
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Congenital origin of the left main coronary artery from the innominate artery in a 37-year-old man with syncope and right ventricular dysplasia. Catheter Cardiovasc Interv. 2001 Mar; 52(3):378-81.