• Presse Med · Jun 1998

    Review

    [Congenital long QT syndrome].

    • J M Lupoglazoff, I Denjoy, N Neyroud, P Guicheney, A Casasoprana, and P Coumel.
    • Service de Cardiologie infantile, Hôpital Robert Debré, Paris. jean-marc.lupoglazof@rdb.ap-hop-paris.fr
    • Presse Med. 1998 Jun 13; 27 (21): 1029-34.

    AbstractSEVERAL 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.

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