Long QT syndrome type 6 (Q85874): Difference between revisions
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Forma autossômica dominante relativamente incomum de LQTS. Envolve mutações no gene KCNE2, que codifica para a subunidade beta do canal de potássio MiRP1, constituindo parte da corrente repolarizante de K+ IKr. | |||
| description / en | description / en | ||
This is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE2, which encodes for the potassium channel beta subunit MiRP1, constituting part of the IKr repolarizing K+ current. | |||
Revision as of 11:14, 15 August 2026
This is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE2, which encodes for the potassium channel beta subunit MiRP1, constituting part of the IKr repolarizing K+ current.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1998894476 |
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| English | Long QT syndrome type 6 |
This is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE2, which encodes for the potassium channel beta subunit MiRP1, constituting part of the IKr repolarizing K+ current. |
