Pyridoxine‐responsive KCNQ2 epileptic encephalopathy: Additional cases and literature review

BACKGROUND: Typical patients with KCNQ2 (OMIM# 602235) epileptic encephalopathy present early neonatal‐onset intractable seizures with a burst suppression EEG pattern and severe developmental delay or regression, and those patients always fail first‐line treatment with sodium channel blockers. Vitam...

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Detalles Bibliográficos
Autores principales: Chen, Jun, Tao, Qiuji, Fan, Lijuan, Shen, Yajun, Liu, Jinfeng, Luo, Huan, Yang, Zuozhen, Liang, Mengmeng, Gan, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544210/
https://www.ncbi.nlm.nih.gov/pubmed/35906921
http://dx.doi.org/10.1002/mgg3.2024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544210/
https://www.ncbi.nlm.nih.gov/pubmed/35906921
http://dx.doi.org/10.1002/mgg3.2024

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