Long QT syndrome type 5 (Q85872): Difference between revisions
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13 August 2026
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Latest revision as of 11:13, 15 August 2026
This is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE1, which encodes for the potassium channel beta subunit MinK. In its rare homozygous forms, it can lead to Jervell and Lange-Nielsen syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1160601997 |
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| English | Long QT syndrome type 5 |
This is an autosomal dominant relatively uncommon form of LQTS. It involves mutations in the gene KCNE1, which encodes for the potassium channel beta subunit MinK. In its rare homozygous forms, it can lead to Jervell and Lange-Nielsen syndrome. |
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CID11:ID_1160601997
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dki-india-ID_1160601997
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Concluído
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13 August 2026
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