LQT9: Difference between revisions
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==Overview== | ==Overview== | ||
LQT9 subtype is a variant of long QT syndrome, which causes abnormalities in a membrane protein called [[caveolin]]. | |||
==LQT9== | ==LQT9== |
Revision as of 17:29, 7 October 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]
Overview
LQT9 subtype is a variant of long QT syndrome, which causes abnormalities in a membrane protein called caveolin.
LQT9
Type | OMIM | Mutation |
LQT9 | Caveolin 3 |
This newly discovered variant is caused by mutations in the membrane structural protein,caveolin-3. Caveolins form specific membrane domains called caveolae in which among others the NaV1.5 voltage-gated sodium channel sits. Similar to LQT3, these particular mutations increase so-called 'late' sodium current which impairs cellular repolarization.