Diagnosis, management and therapeutic strategies for congenital long QT syndrome

Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation and life-threatening arrhythmias, leading to syncope and sudden death. Variations in genes encoding for cardiac ion channels, accessory ion channel subunits or proteins modulating the function of the...

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Detalles Bibliográficos
Autores principales: Wilde, Arthur A M, Amin, Ahmad S, Postema, Pieter G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862104/
https://www.ncbi.nlm.nih.gov/pubmed/34039680
http://dx.doi.org/10.1136/heartjnl-2020-318259

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862104/
https://www.ncbi.nlm.nih.gov/pubmed/34039680
http://dx.doi.org/10.1136/heartjnl-2020-318259

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