Familial long QT syndrome

Description

A rare group of genetic, cardiac rhythm diseases characterized by a prolongation of the QT interval at basal electrocardiography (ECG) and by a high risk of life-threatening arrhythmias.

Cell Lines

ZZUSAHi004-A
STBCi096-A
UKKi008-A
UKKi009-A
UKKi009-B
UKKi016-A
UKKi016-B
UKKi016-C
UKKi018-A
UKKi018-B
UKKi018-C
UKKi019-A
UKKi019-B
UKKi019-C
UKKi023-A
UKKi023-B
UKKi023-C
UKKi029-A
UKKi029-B
UKKi029-C
UKKi034-A
UKKi034-B
UKKi034-C

Link

For more information, please consult the corresponding entry in Orphanet* .

*Orphanet: an online rare disease and orphan drug data base. Copyright, INSERM 1999. Available on http://www.orpha.net.