Work

An Adolescent with Possible Arrhythmogenic Right Ventricular Dysplasia and Long QT Syndrome: Evaluation and Management

Year: 2013

Type: article

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.

Source: Annals of Noninvasive Electrocardiology

DOI: 10.1111/anec.12043

Authors: Svjetlana Tisma‐Dupanovic, Jonathan B. Wagner, Sanket Shah, David T. Huang, Arthur J. Moss

Institutions: University of Missouri–Kansas City, University of Rochester Medicine

Language: English

Topic: Cardiovascular Effects of Exercise

Subfield: Cardiology and Cardiovascular Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funder: Eunice Kennedy Shriver National Institute of Child Health and Human Development