DNM1 Mutation in a child associated with progressive bilateral mesial temporal sclerosis

This case represents a novel association of a DNM1 gene mutation with status epilepticus and progressive bilateral mesial temporal sclerosis. This could have future implications for treatment in patients with DNM1 mutation and refractory epilepsy as the mesial temporal sclerosis may become bilateral...

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Detalles Bibliográficos
Autores principales: Lazzara, Alexandra, Asghar, Sheila, Zacharia, Thomas, Byler, Debra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230638/
https://www.ncbi.nlm.nih.gov/pubmed/30455886
http://dx.doi.org/10.1002/ccr3.1793

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230638/
https://www.ncbi.nlm.nih.gov/pubmed/30455886
http://dx.doi.org/10.1002/ccr3.1793

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