Hereditary Angioedema with Recurrent Abdominal Pain in a Patient with a Novel Mutation
Author:
Affiliation:
1. Emergency and Critical Care Center, Kishiwada Tokushukai Hospital, Japan
2. Department of Internal Medicine, Kyushu University Beppu Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/55/19/55_55.6951/_pdf
Reference13 articles.
1. 1. Bowen T, Cicardi M, Farkas H, et al. 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol 6: 24, 2010.
2. 2. Waytes AT, Rosen FS, Frank MM. Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate. N Engl J Med 334: 1630-1634, 1996.
3. 3. Tosi M. Molecular genetics of C1 inhibitor. Immunobiology 199: 358-365, 1998.
4. 4. Zuraw BL, Herschbach J. Detection of C1 inhibitor mutations in patients with hereditary angioedema. J Allergy Clin Immunol 105: 541-546, 2000.
5. 5. Pappalardo E, Cicardi M, Duponchel C, et al. Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema. J Allergy Clin Immunol 106: 1147-1154, 2000.
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