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- W2895544824 abstract "Introduction: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a malignant genetic disorder of adrenergically-mediated polymorphic ventricular arrhythmias. Traditionally, it has been characterized by absence of structural heart disease. Recent case reports have linked CPVT due to exon 3 deletions in the ryanodine receptor (RYR2) gene to left ventricular noncompaction (LVNC). Hypothesis: We hypothesized that structural heart disease would be evident on cardiac MRI in patients with clinically confirmed CPVT, despite normal echocardiograms. Methods: We performed a retrospective observational analysis of families with CPVT, followed by the Stanford Inherited Arrhythmia Clinic, who had normal echocardiograms. Medical records, cardiac MRIs ordered for clinical indications, and genetic testing results were reviewed. Results: Of 13 patients identified with CPVT, 10 had bidirectional or polymorphic ventricular ectopy on treadmill testing and 69% (9 patients) had suffered an aborted cardiac arrest. G..." @default.
- W2895544824 created "2018-10-12" @default.
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- W2895544824 date "2016-11-11" @default.
- W2895544824 modified "2023-09-26" @default.
- W2895544824 title "Abstract 20771: Occult Structural Disease in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia" @default.
- W2895544824 hasPublicationYear "2016" @default.
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