Arrhythmogenic right ventricular cardiomyopathy
MONDO:0016587Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that consists in progressive dystrophy of primarily the right ventricular myocardium with fibro-fatty replacement and ventricular dilation, and that is clinically characterized by ventricular arrhythmias and a risk of sudden cardiac death.
Also known as: ARVD, arrhythmogenic RVD, arrhythmogenic right ventricular cardiomyopathy, arrhythmogenic right ventricular dysplasia, right ventricular dysplasia
38 clinical trials for this condition and its sub-types, 29 tagged with Arrhythmogenic right ventricular cardiomyopathy itself.
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Sub-types of Arrhythmogenic right ventricular cardiomyopathy
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Familial isolated arrhythmogenic right ventricular dysplasia 0 trials · 10 incl. sub-types
16 sub-types
- Arrhythmogenic right ventricular dysplasia 9 5 trials
- Arrhythmogenic right ventricular dysplasia 1 3 trials
- Familial isolated arrhythmogenic ventricular dysplasia, left dominant form 3 trials
- Catecholaminergic polymorphic ventricular tachycardia 1 2 trials
- Arrhythmogenic right ventricular dysplasia 10 0 trials
- Arrhythmogenic right ventricular dysplasia 11 0 trials
- Arrhythmogenic right ventricular dysplasia 12 0 trials
- Arrhythmogenic right ventricular dysplasia 13 0 trials
- Arrhythmogenic right ventricular dysplasia 3 0 trials
- Arrhythmogenic right ventricular dysplasia 4 0 trials
- Arrhythmogenic right ventricular dysplasia 5 0 trials
- Arrhythmogenic right ventricular dysplasia 6 0 trials
- Arrhythmogenic right ventricular dysplasia 8 0 trials
- Arrhythmogenic right ventricular dysplasia, familial, 14 0 trials
- Familial isolated arrhythmogenic ventricular dysplasia, biventricular form 0 trials
- Familial isolated arrhythmogenic ventricular dysplasia, right dominant form 0 trials
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Naxos disease 0 trials