Homozygous TBC1D24 Mutation in a Case of Epilepsia Partialis Continua

TBC1D24 mutation-related epileptic syndrome includes a wide spectrum of epilepsies. We describe a case with a homozygous TBC1D24 mutation inherited from consanguineous parents. The patient manifested epilepsia partialis continua (EPC) and rare secondary generalized tonic–clonic seizure without intel...

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Detalles Bibliográficos
Autores principales: Zhou, Qilin, Lin, Yicong, Ye, Jing, Li, Liping, Hu, Ningning, Wang, Di, Wang, Yuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787533/
https://www.ncbi.nlm.nih.gov/pubmed/29416524
http://dx.doi.org/10.3389/fneur.2017.00750

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787533/
https://www.ncbi.nlm.nih.gov/pubmed/29416524
http://dx.doi.org/10.3389/fneur.2017.00750

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