作者: Tom Bowen , Jacques Hebert , Bruce Ritchie , Jeanne Burnham , Mike MacSween
DOI: 10.1016/J.TRANSCI.2003.08.009
关键词:
摘要: Abstract C1 esterase inhibitor (C1-INH) deficiency is a rare disorder that lacks consensus for diagnosis therapy and management. Recognizing Canada behind the European approach to this disorder, we have formed Canadian Hereditary Angioedema Society (CHAES)/Societe d'angioedeme hereditaire du (SAHC) foster knowledge of in advance care patients with Canada. We here present review treatment including prevention angioedema events use replacement an algorithm management C1-INH discussion at our International Conference on be held Toronto, Canada, October 24th 26th, 2003.