A deep learning approach identifies new ECG features in congenital long QT syndrome

BACKGROUND: Congenital long QT syndrome (LQTS) is a rare heart disease caused by various underlying mutations. Most general cardiologists do not routinely see patients with congenital LQTS and may not always recognize the accompanying ECG features. In addition, a proportion of disease carriers do no...

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Detalles Bibliográficos
Autores principales: Aufiero, Simona, Bleijendaal, Hidde, Robyns, Tomas, Vandenberk, Bert, Krijger, Christian, Bezzina, Connie, Zwinderman, Aeilko H., Wilde, Arthur A. M., Pinto, Yigal M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063181/
https://www.ncbi.nlm.nih.gov/pubmed/35501785
http://dx.doi.org/10.1186/s12916-022-02350-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063181/
https://www.ncbi.nlm.nih.gov/pubmed/35501785
http://dx.doi.org/10.1186/s12916-022-02350-z

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