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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Dades bibliogràfiques
Publicat a:Epilepsy Behav Rep
Autors principals: Ikeda, Azusa, Yamamoto, Ayako, Ichikawa, Kazushi, Tsuyusaki, Yu, Tsuji, Megumi, Iai, Mizue, Enomoto, Yumi, Murakami, Hiroaki, Kurosawa, Kenji, Miyatake, Satoko, Matsumoto, Naomichi, Goto, Tomohide
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2019
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Article
Accés en línia: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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