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Mesh term Long QT Syndrome

Browse to parent terms:
Arrhythmias, Cardiac
Cardiac Conduction System Disease
Heart Defects, Congenital

Description

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 and JERVELL-LANGE NIELSEN SYNDROME.


Browse to child terms:
Andersen Syndrome
Jervell-Lange Nielsen Syndrome
Romano-Ward Syndrome


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