
First case of homozygous C1 inhibitor deficiency
Keywords: C1 بازدارنده; Hereditary angioedema; C1 inhibitor; classical complement activation pathway; serine protease inhibitor; homozygous C1NH mutationAAE, Acquired angioedema; C1-Inh, C1 inhibitor protein; C1NH, C1 inhibitor gene; HAE, Hereditary angioedema; RF, Rheumatoid fa