A delayed diagnosis of catecholaminergic polymorphic ventricular tachycardia with a mutant of RYR2 at c.7580T>G for 6 years in a 9-year-old child
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference15 articles.
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3. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: the Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC);Priori;Eur Heart J,2015
4. Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia;Hayashi;Circulation,2009
5. Catecholaminergic polymorphic ventricular tachycardia (CPVT) associated with ryanodine receptor (RyR2) gene mutations—long-term prognosis after initiation of medical treatment;Kawata;Circ J,2016
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3. Correction: “Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?;Cell Death & Disease;2022-11-30
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