ヤマモト トシユキ
Yamamoto Toshiyuki
山本 俊至 所属 医学部 医学科(東京女子医科大学病院) 職種 教授 |
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論文種別 | 症例報告 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Late-onset epileptic spasms in a patient with 22q13.3 deletion syndrome. |
掲載誌名 | 正式名:American Journal of Medical Genetics. Part A 略 称:Am J Med Genet A ISSNコード:15524825/15524833 |
掲載区分 | 国外 |
巻・号・頁 | 38(1),pp.109-112 |
著者・共著者 | Ishikawa N, Kobayashi Y, Fujii Y, Yamamoto T, Kobayashi M. |
発行年月 | 2015/01 |
概要 | Patients with 22q13.3 deletion syndrome present with diverse neurological problems such as global developmental delays, hypotonia, delayed or absent speech, autistic behavior, and epilepsy. Seizures occur in up to one-third of patients with 22q13.3 deletion syndrome; however, only a few reports have provided details regarding the seizure manifestations. The present report describes a patient with 22q13.3 deletion syndrome who presented with late-onset epileptic spasms (ES) and electroencephalography features like Lennox-Gastaut syndrome. An array comparative genomic hybridization analysis revealed that a chromosomal deletion of this patient included SHANK3. To the best of our knowledge, this is the first confirmed case of late-onset ES occur in patients with 22q13.3 deletion syndrome with a SHANK3 deletion. |
DOI | 10.1016/j.braindev.2015.06.002 |
PMID | 26094094 |