TANGO2 : A Rare but Important Mutation

• Published in: The Journal of innovations in cardiac rhythm management (Print) 2024-06, Vol.15 (5), p.5871-5875
• Main Authors: Walters, Benjamin, McConkey, Nathan, Imundo, Jason R
• Format: Article
• Language: English
• Subjects: Case Report
• ISSN: 2156-3977; 2156-3993
• DOI: 10.19102/icrm.2024.15054

We report the case of a 7-year-old boy who presented with post-viral myositis, rhabdomyolysis, and hepatitis, who was later readmitted due to a seizure-like activity and ultimately found to have episodes of recalcitrant polymorphic ventricular tachycardia secondary to simultaneous QT prolongation and severe hypothyroidism. Temporary transvenous atrial pacing was successful at controlling the ventricular arrhythmias in the intensive care unit. With levothyroxine therapy and cessation of QT-prolonging medications, the corrected QT (QTc) normalized. A comprehensive arrhythmia panel identified a pathogenic mutation in , consistent with long QT syndrome (LQTS) type 1. After the patient experienced progressive neurodegeneration and seizures, he was referred to a genetics clinic to rule out genetic epilepsy. On the epilepsy panel of genetic testing, he was found to have two pathogenic variants in . deficiency explains the initial presentation of myositis, rhabdomyolysis, hypothyroidism, and life-threatening arrhythmias surrounding a viral illness more so than the initial diagnosis of mere LQTS. However, the gene is not included in most comprehensive arrhythmia and cardiomyopathy panels. deficiency is a rare condition that often presents with arrhythmias but may be unfamiliar to many cardiologists and electrophysiologists. This case describes management strategies and caveats, which could aid in the successful diagnosis and treatment of deficiency at the time of presentation.