Cardiocerebral channelopathy caused by KCND3 mutation in a child: A case report

Early repolarization syndrome is rare in children. Mutation of genes encoding ion channels could display mixed electrophysiological phenotype of Kv4.3 including both cardiac phenotype (early repolarization syndrome, atrial fibrillation) and cerebral phenotype (epilepsy, intellectual disability). Thi...

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Detalles Bibliográficos
Autores principales: Zhang, Yi, Jiang, He, Li, Xiao-mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742191/
https://www.ncbi.nlm.nih.gov/pubmed/36518774
http://dx.doi.org/10.3389/fped.2022.1019122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742191/
https://www.ncbi.nlm.nih.gov/pubmed/36518774
http://dx.doi.org/10.3389/fped.2022.1019122

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