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, v...
Topics
- Adrenergic beta-Antagonists
- Deafness
- Electrocardiography, Ambulatory
- Female
- Genotype
- Humans
- Long QT Syndrome
- Male
- Phenotype
- Prognosis
- Torsades de Pointes
