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Title: [Hereditary angioedema. A hereditary disorder in the synthesis of the complement system]. Author: Vanderstock L, Vander Eecken P, Vermeersch H. Journal: Acta Otorhinolaryngol Belg; 1983; 36(3):418-31. PubMed ID: 6613563. Abstract: Hereditary angioedema is characterized by recurrent attacks of painless, non itching edema of the face and limbs and sometimes by abdominal symptoms. It is due to a deficiency of functional inhibitor of the first component of complement (C1 Inh). We present a case where a normal antigenic level of C1 Inh was found but no functional activity was present (B variant). A short review is given of the pathogenesis, heredity, diagnosis and treatment of the disease.[Abstract] [Full Text] [Related] [New Search]