Epilepsy in patients with long QT syndrome type 1: A Norwegian family

The congenital long QT syndrome (cLQTS) is an inherited cardiac disorder and is associated with sudden cardiac death. We describe a Norwegian family with mutations within the KCNQ1 gene causing cLQTS type 1 (LQT1) and epilepsy. The index patient had Jervell and Lange-Nielsen-syndrome (JLNS) with dea...

Descripción completa

Detalles Bibliográficos
Autores principales: González, Alba, Aurlien, Dag, Haugaa, Kristina H., Taubøll, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215028/
https://www.ncbi.nlm.nih.gov/pubmed/30406014
http://dx.doi.org/10.1016/j.ebcr.2018.09.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215028/
https://www.ncbi.nlm.nih.gov/pubmed/30406014
http://dx.doi.org/10.1016/j.ebcr.2018.09.006

Ejemplares similares