National prevalence survey of hereditary angioedema in Japan

Japanese Journal of Allergology

Volumn 60, Issue 1, 2011, Pages 26-32

  Iwamoto, Kazumasa ^a   Mihara, Shoji ^a   Ikezawa, Zenro ^b   Hide, Michihiro ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

^b YOKOHAMA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Angioedema; C1 inhibitor; Hereditary angioedema; Japanese; National prevalence survey

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR;

ABDOMINAL DISCOMFORT; ANGIONEUROTIC EDEMA; ARTICLE; CLINICAL TRIAL; DERMATOLOGY; HEALTH SURVEY; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MULTICENTER STUDY; PREVALENCE; QUESTIONNAIRE; SKIN SWELLING; THROAT DISEASE;

ANGIOEDEMAS, HEREDITARY; COMPLEMENT C1 INHIBITOR PROTEIN; DANAZOL; HUMANS; JAPAN; PREVALENCE; TRANEXAMIC ACID;

EID: 79952552478     PISSN: 00214884     EISSN: 13477935     Source Type: Journal    
DOI: None     Document Type: Article

References (17)

1. Bowen T, Cicardi M, Bork K, Zuraw B, Frank M, Ritchie B, et al. Hereditary angiodema a current state-of-the-art review VII Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis Therapy and Management of Hereditary Angioedema Ann Allergy Asthma Immunol 2008; 100: S30-40.
2. Pappalardo E, Cicardi M, Duponchel C, Carugati A, Choquet S, Agostoni A, et al. Frequent de novo mutations and exon deletions in the C1 inhibitor gene of patients with angioedema. J Allergy Clin Immunol 2000; 106: 1147-54. (Pubitemid 32006270)
3. Medical Torch 2009; 5: 28-31.
4. Gompels MM, Lock RJ, Abinun M, Bethune CA, Davies G, Grattan C, et aL C1 inhibitor deficiency: consensus document. Clin Exp Immunol 2005; 139: 379-94.
5. Ren HL, Zhang HY. Clinical features of hereditary angioedema: analysis of 133 cases. Zhonghua Yi Xue Za Zhi 2007; 87: 2772-6.
6. Yu TC, Shyur SD, Huang LH, Wen DC, Li JS. Paternal mosaicism and hereditary angioedema in a Taiwanese family. Ann Allergy Asthma Immunol 2007; 99: 375-9.
7. Kang HR, Yim EY, Oh SY, Chang YS, Kim YK, Cho SH, et al. Normal C1 inhibitor mRNA expression level in type I hereditary angioedema patients: newly found C1 inhibitor gene mutations. Allergy 2006: 61: 260-4. (Pubitemid 43381840)
8. 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.
9. Frank MM, Gelfand JA, Atkinson JP. Hereditary angioedema: the clinical syndrome and its management Ann Intern Med 1976; 84: 580-93.
10. Visual Dermatology 2005; 4: 710-1.
11. Waytes AT, Rosen FS, Frank MM. Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate. N Engl J Med 1996; 334: 1630-4. (Pubitemid 26192522)
12. http://square.umin.ac.jp/compl/HAE/HAEGuideline.html
13. Zuraw BL. Clinical practice. Hereditary angioedema N Engl J Med 2008; 359: 1027-36.
14. Sheffer AL, Austen KF, Rosen FS. Tranexamic acid therapy in hereditary angioneurotic edema N Engl J Med 1972; 287: 452-4.