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Long QT syndrome

MONDO:0002442

A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome.

Also known as: long QT syndrome, ventricular arrhythmia associated with long QT syndrome

25 clinical trials for this condition and its sub-types.

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Sub-types

Long QT syndrome 3 (5) Long QT syndrome 2 (3) Jervell and Lange-Nielsen syndrome (2) Jervell and Lange-Nielsen syndrome 1 (1) Jervell and Lange-Nielsen syndrome 2 (1) Long QT syndrome 1 (1) Timothy syndrome (1) Timothy syndrome type 1 (1) Andersen-Tawil syndrome (0) Cardiac arrhythmia, ankyrin-B-related (0) Familial long QT syndrome (0) Long QT syndrome 10 (0) Long QT syndrome 11 (0) Long QT syndrome 12 (0) Long QT syndrome 13 (0) Long QT syndrome 14 (0) Long QT syndrome 15 (0) Long QT syndrome 16 (0) Long QT syndrome 4 (0) Long QT syndrome 5 (0)

Broader categories

Disease (618) Syndromic disease (24) Human disease (14) Disease by body system or component (0)
Trials to join now! 13 Not yet recruiting 3 Not yet finished but already full! 4 Completed 4 Terminated 1
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