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Neonatal complex arrhythmias possibly related to a TTN mutation
Journal article   Peer reviewed

Neonatal complex arrhythmias possibly related to a TTN mutation

William N Evans, Ruben J Acherman, Ian H Law, Nicholas H Von Bergen, Ricardo A Samson and Humberto Restrepo
Journal of neonatal-perinatal medicine, Vol.10(3), pp.343-346
2017
DOI: 10.3233/NPM-16120
PMID: 28854511

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Abstract

We describe a neonate born with complex arrhythmias that included concurrent atrial and ventricular tachycardias. Genetic testing demonstrated a mutation in the TTN gene, which codes for titin, a large protein found in striated muscle sarcomeres. The complex arrhythmias were successfully treated with amiodarone and flecainide. The patient remains asymptomatic with normal biventricular function. We speculate that the complex arrhythmias and TTN gene mutation may be related.
Tachycardia, Supraventricular - drug therapy Tachycardia, Supraventricular - genetics Tachycardia, Ventricular - drug therapy Humans Connectin - genetics Anti-Arrhythmia Agents - therapeutic use Bundle-Branch Block - diagnosis Bundle-Branch Block - genetics Bundle-Branch Block - drug therapy Tachycardia, Supraventricular - diagnosis Amiodarone - therapeutic use Infant, Premature Tachycardia, Ventricular - diagnosis Electrocardiography Tachycardia, Ventricular - genetics Mutation Infant, Newborn Fetal Monitoring Flecainide - therapeutic use

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