Epilepsy in Christianson syndrome: Two cases of Lennox–Gastaut syndrome and a review of literature

Christianson syndrome (CS) is an X-linked intellectual disorder caused by mutations in the SLC9A6 gene. Clinical features of CS include an inability to speak, truncal ataxia, postnatal microcephaly, hyperkinesis, and epilepsy. Almost all patients with CS develop drug-resistant epilepsy—its most seri...

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Detalles Bibliográficos
Autores principales: Ikeda, Azusa, Yamamoto, Ayako, Ichikawa, Kazushi, Tsuyusaki, Yu, Tsuji, Megumi, Iai, Mizue, Enomoto, Yumi, Murakami, Hiroaki, Kurosawa, Kenji, Miyatake, Satoko, Matsumoto, Naomichi, Goto, Tomohide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920258/
https://www.ncbi.nlm.nih.gov/pubmed/31879735
http://dx.doi.org/10.1016/j.ebr.2019.100349

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