文献

J-GLOBAL ID：202002232563449705   整理番号：20A2808687

正常なC1-INHのHAEでのてんかんの高い有病率

High prevalence of epilepsy in HAE with normal C1-INH

著者 (9件)： Kuwahara Saki (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Fukunaga Atsushi (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Ohata Marie (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Nakatani Shoko (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Yokoyama Daisuke (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Nakauchi Emi (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Yoshioka Ai (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine) ,  Kinoshita Masako (Department of Neurology, National Hospital Organization Utano National Hospital) ,  Nishigori Chikako (Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine)
資料名： Allergology International  (Allergology International)
巻： 69  号： 4  ページ： 630-632(J-STAGE)  発行年： 2020年 
JST資料番号： L6446A  ISSN： 1323-8930  資料種別： 逐次刊行物 (A)
記事区分： 短報  発行国： 日本 (JPN)  言語： 英語 (EN)

抄録/ポイント： ・C1阻害因子(C1-INH)欠損型遺伝性血管浮腫(HAE)...

シソーラス用語： *遺伝病 ,...
準シソーラス用語： C1阻害剤 ,...

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分類 (2件)： 循環系の疾患  (GJ03000C) ,  神経系の疾患  (GN03000O)

引用文献 (16件)：

• 1. Agostoni A, Cicardi M. Hereditary and acquired C1-inhibitor deficiency: biological and clinical characteristics in 235 patients. Medicine (Baltimore) 1992;71:206-15.
• 2. Zuraw BL. Hereditary angioedema with normal C1 inhibitor: four types and counting. J Allergy Clin Immunol 2018;141:884-5.
• 3. Bork K, Wulff K, Rossmann H, Steinmüller-Magin L, Braenne I, Witske G, et al. Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin. Allergy 2019;74:2479-81.
• 4. Bork K, Meng G, Staubach P, Hardt J. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. Am J Med 2006;119:267-74.
• 5. Chung JY, Kim M. Migraine-like headache in a patient with complement 1 inhibitor deficient hereditary angioedema. J Korean Med Sci 2012;27:104-6.

タイトルに関連する用語 (4件)： C1 ,  INH ,  てんかん ,  有病率