A Case of Hereditary Angioedema Involving Recurrent Abdominal Attacks
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概要
- 論文の詳細を見る
A 44-year-old Japanese woman was diagnosed with type 1 hereditary angioedema (HAE) at the age of 30. In March 2007, she began suffering from severe abdominal pain due to intestinal edema. After treatment with C1-INH concentrate, her symptoms disappeared. However, during the subsequent three years, the frequency of the attacks increased continuously, and C1-INH concentrate was necessary for treatment of every attack. The increase in the number of attacks might have been due to the frequent injection of C1-INH concentrate or the deterioration of her disease course. In a genetic investigation, the patient was found to have a novel mutation in the C1-INH gene.
- 社団法人 日本内科学会の論文
著者
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Horiuchi Takahiko
Department Of Medicine And Biosystemic Science Graduate School Of Medical Sciences Kyushu University
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Kasamatsu Yu
Department Of Internal Medicine Osaka City General Hospital
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Kadoya Masatoshi
Department Of Surgery Sapporo Minamisanjo Hospital
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Kasamatsu Yu
Department of Respiratory Medicine, Matsushita Memorial Hospital, Japan
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Kasamatsu Yoshihiro
Department of Respiratory Medicine, Matsushita Memorial Hospital, Japan
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Yoshinoya Kiyokazu
Department of Respiratory Medicine, Matsushita Memorial Hospital, Japan
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Yamamoto Tetsuro
YAMAMOTO CLINIC, Japan
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