The long QT syndrome. Prospective longitudinal study of 328 families. | Zendy

Arthur J. Moss | Zendy; Peter J. Schwartz | Zendy; Richard S. Crampton | Zendy; Dan Tzivoni | Zendy; Emanuela H. Locati | Zendy; J. W. MacCluer | Zendy; William J. Hall | Zendy; L. Weitkamp | Zendy; G. Michael Vincent | Zendy; Arthur Garson | Zendy

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The long QT syndrome. Prospective longitudinal study of 328 families.

Author(s) -

Arthur J. Moss,

Peter J. Schwartz,

Richard S. Crampton,

Dan Tzivoni,

Emanuela H. Locati,

J. W. MacCluer,

William J. Hall,

L. Weitkamp,

G. Michael Vincent,

Arthur Garson

Publication year - 1991

Publication title -

circulation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 7.795

H-Index - 607

eISSN - 1524-4539

pISSN - 0009-7322

DOI - 10.1161/01.cir.84.3.1136

Subject(s) - medicine , long qt syndrome , proband , qt interval , syncope (phonology) , cardiology , sudden death , pediatrics , sudden cardiac death , prospective cohort study , biochemistry , chemistry , mutation , gene

The Long QT Syndrome (LQTS) is an infrequently occurring familial disorder in which affected individuals have electrocardiographic QT interval prolongation and a propensity to ventricular tachyarrhythmic syncope and sudden death. We prospectively investigated the clinical characteristics and the long-term course of 3,343 individuals from 328 families in which one or more members were identified as affected with LQTS (QTc greater than 0.44 sec1/2).

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