Quinidine Therapy for Lennox-Gastaut Syndrome With KCNT1 Mutation. A Case Report and Literature Review

Mutations in the Potassium channel subfamily T member 1 (KCNT1) gene have been reported in a range of epileptic encephalopathies. Here we report the case of a 12-year-old male suffering from multiple types of epileptic seizures and cognitive decline from the age of 10. The patient had four types of...

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Dades bibliogràfiques
Publicat a:Front Neurol
Autors principals: Jia, Yu, Lin, Yicong, Li, Jing, Li, Mingyu, Zhang, Yifan, Hou, Yue, Liu, Aihua, Zhang, Liping, Li, Liping, Xiang, Peng, Ye, Jing, Huang, Zhaoyang, Wang, Yuping
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2019
Matèries:
Neurology
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6370615/
https://ncbi.nlm.nih.gov/pubmed/30804880
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.00064
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