カルバマゼピン投与によるミオクロニー発作増悪時にDoose症候群と診断しエトスクシミドが著効した3歳男児
Author:
Affiliation:
1. Department of Pediatrics, Nippon Medical School, Musashi Kosugi Hospital
2. Department of Pediatrics, St. Marianna University School of Medicine
3. Department of Pediatrics, Nippon Medical School, Tama Nagayama Hospital
Publisher
Medical Association of Nippon Medical School
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
https://www.jstage.jst.go.jp/article/manms/19/2/19_171/_pdf
Reference10 articles.
1. 1. Wirrell EC, Grossardt BR, Wong-Kisiel LC, Nickels KC: Incidence and classification of new-onset epilepsy and epilepsy syndromes in children in Olmsted County, Minnesota from 1980 to 2004: a population-based study. Epilepsy Research 2011; 95: 110-118.
2. 2. 小国 弘量: Doose症候群. 稀少難治てんかん診療マニュアル-疾患の特徴と診断のポイント. 大槻 泰介, 須貝 研司, 小国 弘量, 井上 有史, 永井 利三郎編. 2013; pp 15-17, 診断と治療社 東京.
3. 3. Tang S, Addis L, Smith A, et al.: Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures. Epilepsia 2020; 61: 995-1007.
4. 4. Oguni H, Tanaka T, Hayashi K, et al.: Treatment and Long-Term Prognosis of Myoclonic-Astatic Epilepsy of Early Childhood. Neuropediatrics 2002; 33: 122-132.
5. 5. Oguni H: Epilepsy with myoclonic-atonic seizures also known as Doose syndrome: Modification of the diagnostic criteria. European Journal of Paediatric Neurology 2022; 36: 37-50.
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