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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  SCN5A  gene mutation variant was found leading to diagnosis of sodium-channel dysfunction arrhythmia.

Life Threatening Broad QRS Tachycardia in an Infant with Conduction Disorder and SCN5A Mutation