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Article

Clinical management of patients with the long QT syndrome: drugs, devices, and gene-specific therapy.

Pacing and clinical electrophysiology : PACE - 1 Aug 1997

Moss A J

Abstract excerpt

The familial long QT syndrome (LQTS) is now recognized as a genetic channelopathy with a propensity to arrhythmogenic syncope and sudden death. Three genetic mutations have been identified that involve the slow and fast delayed potassium rectifier currents and the sodium current. Distinctive ECG-T wave phenotypes are associated with each of the three genotypes. Current day therapy includes: beta-adrenergic...

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Identifiers

PMID: 9272508
DOI: 10.1111/j.1540-8159.1997.tb03627.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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