Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis.

PURPOSE: Choreoacanthocytosis (ChAc) is an autosomal recessive disorder caused by mutations in VPS13A on chromosome 9q21 and characterized by neurodegeneration and red cell acanthocytosis. Seizures are not uncommon in ChAc but have not been well characterized in the literature. We report two ChAc f...

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書誌詳細
主要な著者: Al-Asmi, A, Jansen, A, Badhwar, A, Dubeau, F, Tampieri, D, Shustik, C, Mercho, S, Savard, G, Dobson-Stone, C, Monaco, A, Andermann, F, Andermann, E
フォーマット: Journal article
言語:English
出版事項: 2005

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