[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 2006, 32(3) 198-200 DOI:     ISSN: 2096-5540 CN: 32-1880/R

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PubMed
Article by JIANG Jian-xiong
Article by ZHENG Min

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Advances in Hereditary Angioedema

Department of Dermatology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China

Department of Dermatology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China

Abstract:

Hereditary angioedema (HAE) is an autosomal dominant genetic disease caused by synthesis defect or dysfunction of C1 esterase inhibitor. Up to now, no satisfactory treatment is available for the disease, but recent studies indicate that the major mediator of angioedema is bradykinin, thus the plasma kallikrein inhibitor and the bradykinin 2 receptor (Bk2R) antagonist have become the hot spot of new drug investigation, and may provide clinicians with more therapeutic choices. The etiology, pathogenesis, clinical manifestations, as well as treatment of the disease are summarized.

Keywords: Angioneurotic edema   C1 esterase inhibitor   Bradykinin   Therapy  
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