LQT10: Difference between revisions
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==Overview== | ==Overview== | ||
==LQT10== | |||
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| '''Type''' || '''OMIM''' || '''Mutation''' | |||
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| [[LQT10]] || || [[SCN4B]] || | |||
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This novel susceptibility gene for LQT is ''SCN4B'' encoding the protein Na<sub>V</sub>β4, an auxiliary [[subunit]] to the pore-forming Na<sub>V</sub>1.5 (gene: ''SCN5A'') subunit of the [[voltage-gated sodium channel]] of the heart. The mutation leads to a positive shift in inactivation of the sodium current, thus increasing sodium current. Only one mutation in one patient has so far been found. | |||
==References== | ==References== |
Revision as of 17:35, 7 October 2012
Long QT Syndrome Microchapters |
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Treatment |
Case Studies |
LQT10 On the Web |
American Roentgen Ray Society Images of LQT10 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]
Overview
LQT10
Type | OMIM | Mutation | |
LQT10 | SCN4B |
This novel susceptibility gene for LQT is SCN4B encoding the protein NaVβ4, an auxiliary subunit to the pore-forming NaV1.5 (gene: SCN5A) subunit of the voltage-gated sodium channel of the heart. The mutation leads to a positive shift in inactivation of the sodium current, thus increasing sodium current. Only one mutation in one patient has so far been found.