@Article{chd.2022.023711,
AUTHOR = {Elio Caruso, Silvia Farruggio, Alfredo Di Pino, Paolo Guccione, Mohammadrafie Khorgami},
TITLE = {Life Threatening Broad QRS Tachycardia in an Infant with Conduction Disorder and <i>SCN5A</i> Mutation},
JOURNAL = {Structural and Congenital Heart Disease},
VOLUME = {17},
YEAR = {2022},
NUMBER = {5},
PAGES = {551--556},
URL = {http://www.techscience.com/schd/v17n5/49563},
ISSN = {3071-1738},
ABSTRACT = {We present the case of an infant admitted to our department for a rapid broad complex tachycardia and cardiovascular collapse. The patient was submitted to genetic testing because of a conduction defect at baseline ECG
and family history of gene mutation. A new <i>SCN5A</i> gene mutation variant was found leading to diagnosis of
sodium-channel dysfunction arrhythmia.},
DOI = {10.32604/chd.2022.023711}
}