Article
[Congenital long QT syndrome].
Presse medicale (Paris, France : 1983) - 13 Jun 1998
Lupoglazoff J M, Denjoy I, Neyroud N, Guicheney P, Casasoprana A, Coumel P
Abstract excerpt
SEVERAL FORMS: Congenital long QT syndrome is a clinically (with and without deafness) and genetically (recessive or dominant autosomal inheritance) heterogeneous entity characterized by a long QT interval on the ECG associated with the risk of severe ventricular arrhythmia (torsade de pointes, ventricular fibrillation) and subsequent syncope or sudden death. GENETIC DATA: This rare familial syndrome is...
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