Family long QT syndrome type 2 associated with KCNH2 gene mutation: aborted sudden cardiac death
A complete screening was performed in a family after one of its members presented with a sudden cardiac death event. A genetical analysis revealed a mutation which led to a long QT syndrome.
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Veröffentlicht in: | Monaldi archives for chest disease 2023-09 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A complete screening was performed in a family after one of its members presented with a sudden cardiac death event. A genetical analysis revealed a mutation which led to a long QT syndrome. |
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ISSN: | 1122-0643 2532-5264 |
DOI: | 10.4081/monaldi.2023.2663 |