An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and management.

Creator(s)

Svjetlana Tisma-Dupanovic, Children's Mercy HospitalFollow
Jonathan B. Wagner, Children's Mercy HospitalFollow
Sanket Shah, Children's Mercy HospitalFollow
David T. Huang
Arthur J. Moss

Document Type

Article

Publication Date

1-1-2013

Identifier

DOI: 10.1111/anec.12043

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.

Journal Title

Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc

Volume

18

Issue

1

First Page

75

Last Page

78

MeSH Keywords

Adolescent; Adrenergic beta-Antagonists; Arrhythmogenic Right Ventricular Dysplasia; Cardiac Catheterization; Catheter Ablation; Diagnosis, Differential; Echocardiography; Electrocardiography; Exercise Test; Genetic Testing; Humans; Long QT Syndrome; Magnetic Resonance Imaging; Male; Mutation

Keywords

Adolescent; Adrenergic beta-Antagonists; Arrhythmogenic Right Ventricular Dysplasia; Cardiac Catheterization; Catheter Ablation; Diagnosis, Differential; Echocardiography; Electrocardiography; Exercise Test; Genetic Testing; Humans; Long QT Syndrome; Magnetic Resonance Imaging; Male; Mutation

Recommended Citation

Tisma-Dupanovic, S., Wagner, J. B., Shah, S., Huang, D. T., Moss, A. J. An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and management. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 18, 75-78 (2013).