Article
Congenital long QT syndrome presenting as unexplained bradycardia.
BMJ case reports - 2 Mar 2022
Ataíde Silva Rita, R Sousa Ana, de Carvalho Maria Salomé Leal, Anjos Rui
Abstract excerpt
Congenital long QT syndrome (LQTS) is a genetically autosomal heterogeneous disorder of the ion channels and causes about 10% of sudden death infant syndrome in newborns. Its estimated prevalence is approximately 1 in 2500, probably underestimated because of its clinical heterogenicity. Few cases of neonatal LQTS have been reported. In 4% of them, life-threatening arrhythmic events can be the first manifestation...
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