WEKO3
アイテム
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幼児期に発症し,両側大脳白質病変,難治性てんかんを合併したParry-Romberg症候群の1例(<特集>小児科学教室大澤真木子教授開講5周年記念)
http://hdl.handle.net/10470/25188
http://hdl.handle.net/10470/25188f94b19dc-ee03-4c25-b6d8-8aec4e590f8f
名前 / ファイル | ライセンス | アクション |
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KJ00006020638.pdf (1.1 MB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2010-08-10 | |||||
タイトル | ||||||
タイトル | 幼児期に発症し,両側大脳白質病変,難治性てんかんを合併したParry-Romberg症候群の1例(<特集>小児科学教室大澤真木子教授開講5周年記念) | |||||
言語 | ||||||
言語 | jpn | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
別タイトル | ||||||
その他のタイトル | A Case of Early Onset Parry-Romberg Syndrome with Bilateral White Matter Abnormalities and Intractable Epilepsy(Papers for Cerebrating the Fifth Aniversary of the Directorship of Prof. M. Osawa at the Department of Pediatrics, Tokyo Women's Medical University) | |||||
著者名 |
白川, 清吾
× 白川, 清吾× 今井, 薫× 立川, 恵美子× 舟塚, 真× 林, 北見× 小国, 弘量× 大澤, 真木子× 梶本, 美智子× 三浦, 寿男 |
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著者別名 | ||||||
姓名 | SHIRAKAWA, Seigo | |||||
著者別名 | ||||||
姓名 | IMAI, Kaoru | |||||
著者別名 | ||||||
姓名 | TACHIKAWA, Emiko | |||||
著者別名 | ||||||
姓名 | FUNATSUKA, Makoto | |||||
著者別名 | ||||||
姓名 | HAYASHI, Kitami | |||||
著者別名 | ||||||
姓名 | OGUNI, Hirokazu | |||||
著者別名 | ||||||
姓名 | OSAWA, Makiko | |||||
著者別名 | ||||||
姓名 | KAJIMOTO, Michiko | |||||
著者別名 | ||||||
姓名 | MIURA, Hisao | |||||
出版者 | ||||||
出版者 | 東京女子医科大学学会 | |||||
受付日付 | ||||||
日付 | 2010-08-10 | |||||
日付タイプ | Created | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0040-9022 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00161368 | |||||
書誌情報 |
東京女子医科大学雑誌 巻 70, 号 E1, p. E143-E149, 発行日 2000-06-25 |
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著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | A 7-year-old girl with Parry-Romberg syndrome (progressive hemifacial atrophy) was described. She had cutaneous changes on her right forehead that began at 3 years of age, and slowly progressive hemifacial atrophy. Epileptic seizures were first noted at 6 years of age and were intractable including various type of myoclonic seizure, myoclonic astatic seizure, atypical absence, and generalized tonic clonic seizures. EEG showed frequent bi-frontal dominant diffuse spike and wave activity both when awake and asleep. Brain CT revealed multiple intracranial calcifications and frontal bone change ipsilateral to hemifacial atrophy. MRI revealed increased signals on T2 weighted images mainly in the white matter of the right hemisphere and also in the left temporal lobe. Antinuclear antibody (ANA) was positive in serum and local IgG production in the cerebrospinal fluid was increased. Ketogenic diet provided partially control of her epileptic seizures. Previous descriptions of Parry-Romberg syndrome of early onset complicated with epilepsy were reviewed in relation to the present case, and the etiology, neurological complications and intracranial findings in Parry-Romberg syndrome were discussed. | |||||
注記 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 小児科学教室大澤真木子教授開講5周年記念特集 | |||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部小児科学 | ||||||
著者所属 | ||||||
東京女子医科大学医学部眼科学 | ||||||
著者所属 | ||||||
北里大学小児科 |