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Transfus Apher Sci ; 29(3): 205-14, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14572811

ABSTRACT

C1 esterase inhibitor (C1-INH) deficiency is a rare disorder that lacks consensus for diagnosis therapy and management. Recognizing that Canada is behind the European approach to this disorder, we have formed the Canadian Hereditary Angioedema Society (CHAES)/Société d'angioédème héréditaire du Canada (SAHC) to foster knowledge of this disorder in Canada and to advance care of patients with this disorder in Canada. We here present a review of treatment of this disorder in Canada including prevention of angioedema events and use of replacement therapy and present an algorithm for diagnosis therapy and management of C1-INH deficiency in Canada for discussion at our International Conference on Hereditary Angioedema to be held in Toronto, Canada, October 24th to 26th, 2003.


Subject(s)
Angioedema/therapy , Complement C1 Inactivator Proteins/deficiency , Algorithms , Angioedema/diagnosis , Canada , Congresses as Topic , Guidelines as Topic , Humans , Societies
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