The Role of Focal Epilepsy Features in Defining SCN1A Mutation-positive Dravet Syndrome as Generalized and Focal Epilepsy

BACKGROUND AND PURPOSE: This study was aimed to describe focal epilepsy features of SCN1A mutation-positive Dravet syndrome patients. METHODS: A total of 82 SCN1A mutation-positive patients were reviewed retrospectively (39 boys and 43 girls). Seizure type and electroencephalography (EEG) findings w...

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Detalles Bibliográficos
Autores principales: Ko, Young Jun, Yoo, Il Han, Lee, Jiwon, Lee, Jeehun, Yum, Mi-Sun, Ko, Tae-Sung, Kim, Hunmin, Hwang, Hee, Kim, Soo Yeon, Chae, Jong-Hee, Choi, Ji-Eun, Kim, Ki Joong, Lim, Byung Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Epilepsy Society 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767227/
https://www.ncbi.nlm.nih.gov/pubmed/35087721
http://dx.doi.org/10.14581/jer.21019

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