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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Bibliografiska uppgifter
I publikationen:Epilepsy Behav Rep
Huvudupphovsmän: Ikeda, Azusa, Yamamoto, Ayako, Ichikawa, Kazushi, Tsuyusaki, Yu, Tsuji, Megumi, Iai, Mizue, Enomoto, Yumi, Murakami, Hiroaki, Kurosawa, Kenji, Miyatake, Satoko, Matsumoto, Naomichi, Goto, Tomohide
Materialtyp: Artigo
Språk:Inglês
Publicerad: Elsevier 2019
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6920258/
https://ncbi.nlm.nih.gov/pubmed/31879735
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebr.2019.100349
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