Epilepsy phenotype in patients with Xp22.31 microduplication

The clinical significance of Xp22.31 microduplication is still unclear. We describe a family in which a mother and two children have Xp22.31 microduplication associated with different forms of epilepsy and epileptiform EEG abnormalities. The proband had benign epilepsy with centrotemporal spikes wit...

Descripción completa

Detalles Bibliográficos
Autores principales: Brinciotti, Mario, Fioriello, Francesca, Mittica, Antonio, Bernardini, Laura, Goldoni, Marina, Matricardi, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310737/
https://www.ncbi.nlm.nih.gov/pubmed/30603611
http://dx.doi.org/10.1016/j.ebcr.2018.10.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310737/
https://www.ncbi.nlm.nih.gov/pubmed/30603611
http://dx.doi.org/10.1016/j.ebcr.2018.10.004

Ejemplares similares