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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Detalhes bibliográficos
Publicado no:Epilepsy Behav Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha: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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