Catecholaminergic polymorphic ventricular tachycardia classification: Difference between revisions
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==Classification== | ==Classification== | ||
[[CPVT]] may be classified based upon the underlying pathogenic [[mutation]] into the following subtypes: | [[CPVT]] may be classified based upon the underlying pathogenic [[mutation]] into the following subtypes:<ref name="Sumitomo2016">{{cite journal|last1=Sumitomo|first1=Naokata|title=Current topics in catecholaminergic polymorphic ventricular tachycardia|journal=Journal of Arrhythmia|volume=32|issue=5|year=2016|pages=344–351|issn=18804276|doi=10.1016/j.joa.2015.09.008}}</ref> | ||
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Revision as of 08:13, 23 July 2020
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Catecholaminergic polymorphic ventricular tachycardia Microchapters |
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Differentiating Catecholaminergic polymorphic ventricular tachycardia from other Diseases |
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Catecholaminergic polymorphic ventricular tachycardia classification On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Catecholaminergic polymorphic ventricular tachycardia can be classified based upon the underlying pathogenic mutation.
Classification
CPVT may be classified based upon the underlying pathogenic mutation into the following subtypes:[1]
| Type | OMIM | Gene | Protein | Mode of inheritance | Locus |
|---|---|---|---|---|---|
| CPVT1 | 604772 | RyR2 | Ryanodine receptor 2 | Autosomal dominant | 1q42.1-q43 |
| CPVT2 | 611938 | CASQ2 | Calsequestrin 2 | Autosomal recessive | 1p13.3-p11 |
| CPVT3 | 614021 | Unknown | - | Autosomal recessive | 7p14–p22 |
| CPVT4 | 614916 | CALM1 | Calmodulin 1 | Autosomal dominant | 14q32.11 |
| CPVT5 | 615441 | TRDN | Triadin | Autosomal recessive | 6q22.31 |
References
- ↑ Sumitomo, Naokata (2016). "Current topics in catecholaminergic polymorphic ventricular tachycardia". Journal of Arrhythmia. 32 (5): 344–351. doi:10.1016/j.joa.2015.09.008. ISSN 1880-4276.