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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 | |||||||||||||||||||||||||||||||||||||||||||||||||
�ո����� 2005-09-08 ������ ����淢������ | |||||||||||||||||||||||||||||||||||||||||||||||||
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