Long QT syndrome 11

Common Name(s)

Long QT syndrome 11

Congenital long QT syndrome is electrocardiographically characterized by a prolonged QT interval and polymorphic ventricular arrhythmias (torsade de pointes). These cardiac arrhythmias may result in recurrent syncopes, seizure, or sudden death ({2:Jongbloed et al., 1999}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Long QT syndrome 11" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Long QT syndrome 11" returned 1 free, full-text research articles on human participants. First 3 results:

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.
 

Author(s): M Keating, C Dunn, D Atkinson, K Timothy, G M Vincent, M Leppert

Journal: Am. J. Hum. Genet.. 1991 Dec;49(6):1335-9.

 

The long-QT syndrome (LQT; Ward-Romano syndrome) is a cardiac disorder that is inherited as an autosomal dominant trait. Affected family members suffer from recurrent syncope and sudden death due to ventricular arrhythmias. Recently, we identified a DNA marker on the short arm of ...

Last Updated: 10 Jan 1992

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The terms "Long QT syndrome 11" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

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