Deep brain stimulation in a patient with progressive myoclonic epilepsy and ataxia due to potassium channel mutation (MEAK). A case report and review of the literature

Progressive myoclonic epilepsy (PME) is characterized by prominent myoclonus, generalized tonic-clonic seizures, and less often focal, tonic, or absence seizures. The KCNC1 mutation is responsible for specific clinical phenotype of PME which has been defined as myoclonic epilepsy and ataxia due to p...

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Detalles Bibliográficos
Autores principales: Sobstyl, Michał, Kożuch, Nina, Iwaniuk-Gugała, Magdalena, Stapińska-Syniec, Angelika, Konopko, Magdalena, Jezierski, Paweł
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624572/
https://www.ncbi.nlm.nih.gov/pubmed/37928363
http://dx.doi.org/10.1016/j.ebr.2023.100627

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10624572/
https://www.ncbi.nlm.nih.gov/pubmed/37928363
http://dx.doi.org/10.1016/j.ebr.2023.100627

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