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Article

[Diagnosis, sudden death risk stratification, and treatment of main long QT syndrome molecular-genetic variants].

Kardiologiia - 1 Jan 2011

Shkol'nikova M A, Kharlap M S, Il'darova R A, Bereznitskaia V V, Kalinin L A

Abstract excerpt

Inherited long QT syndrome (LQTS) refers to the primary electrical diseases of the heart. It is characterized by QT prolongation on resting ECG and syncope due to life-threatening ventricular arrhythmias. This review focuses on diagnosis, differential diagnosis, risk stratification of sudden cardiac death, and treatment strategy of patients with most prevalent genetic fOrms of LQTS - LQT1, LQT2 and LQT3, which...

Topics

Anti-Arrhythmia Agents
Death, Sudden, Cardiac
Defibrillators, Implantable
Diagnosis, Differential
Electrocardiography
Genetic Association Studies
Genetic Predisposition to Disease
Genetic Testing
History, 20th Century
History, 21st Century

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Humans

Long QT Syndrome

Medication Therapy Management

Precision Medicine

Risk Assessment

Risk Reduction Behavior

Secondary Prevention

Severity of Illness Index

Source

Identifiers

PMID: 21649595

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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