Lasindrome del QT lungo

Translated title of the contribution: The long QT syndrome

Giovanna Ferrara, Emanuela Berton, Claudio Germani, Pierluigi Marzuillo, Paolo Bonazza, Raffaele D'Alfonso, Egidio Barbi

Research output: Contribution to journalArticlepeer-review

Abstract

The long QT syndrome (LQTS) is an arrhythmogenic syndrome due to cardiac ion channel disorders characterized by prolonged QT interval on ECG (QTc >440 ms for male, >460 ms for female) and the most common presentations are syncope, seizures, cardiac arrest and sudden death. Many different congenital forms have been identified but also an acquired form due to specific drugs, hypokalaemia, or hypomagnesemia is known. Familiarity is the leading risk factor. LQTS should be suspected in case of any syncope in order to perform ECG and start proper therapy. To identify and remove risk factors it is necessary to avoid potentially life-threatening arrhythmia in these patients.

Translated title of the contributionThe long QT syndrome
Original languageItalian
Pages (from-to)33-40
Number of pages8
JournalMedico e Bambino
Volume33
Issue number1
Publication statusPublished - Jan 2014

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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