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
Hauptverfasser: Elizalde Uribe, Iván Alejandro, Mendoza Lagos, Diego, Cazares Diazleal, Aldo César, Andrade Cuellar, Elias Noel, Payró Ramírez, Gerardo
Format: Artikel
Sprache:eng
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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.
ISSN:1122-0643
2532-5264
DOI:10.4081/monaldi.2023.2663