Family long QT syndrome type 2 associated with KCNH2 gene mutation: aborted sudden cardiac death.

Autor: Elizalde Uribe IA; Cardiology Department, National Institute of Medical Science and Nutrition 'Salvador Zubiran', Mexico City. ivanaelizalde22@gmail.com., Mendoza Lagos D; Cardiology Department, National Institute of Medical Science and Nutrition 'Salvador Zubiran', Mexico City. diemdzal@gmail.com., Cazares Diazleal AC; Cardiology Department, National Institute of Medical Science and Nutrition 'Salvador Zubiran', Mexico City. a.czdiazleal@gmail.com., Andrade Cuellar EN; Cardiology Department, Medical National Center '20 de Noviembre', ISSSTE, Mexico City. elias.noel.AC@gmail.com., Payró Ramírez G; Cardiology Department, National Institute of Medical Science and Nutrition 'Salvador Zubiran', Mexico City. dr_payro@azumed.mx.
Jazyk: angličtina
Zdroj: Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace [Monaldi Arch Chest Dis] 2023 Sep 13. Date of Electronic Publication: 2023 Sep 13.
DOI: 10.4081/monaldi.2023.2663
Abstrakt: 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.
Databáze: MEDLINE
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