Related Experiment Video
Updated: May 14, 2026

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and
Svjetlana Tisma-Dupanovic1, Jonathan B Wagner, Sanket Shah
1University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA. stisma@cmh.edu
Abstract:
We describe a unique presentation of arrhythmogenic right ventricular dysplasia (ARVD) in a 14-year-old Caucasian male who was additionally diagnosed with long QT syndrome (LQTS). Genetic testing eventually confirmed the diagnosis of both ARVD and LQTS, which combined, to our knowledge, has not been reported in the literature.
Related Concept Videos
Dysrhythmias V: Evaluating Dysrhythmias
Cardiomyopathy III: Hypertrophic Cardiomyopathy
ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias
Dysrhythmias VI: Management of Dysrhythmias
Cardiomyopathy II: Dilated Cardiomyopathy
Dysrhythmias VII: Nursing Management of Dysrhythmias

