Type I hereditary angio‐oedema. Variability of clinical presentation and course within two large kindreds - WINNEWISSER, J.; ROSSI, M.; SPÄTH, P.; BÜRGI, H. (Journal of internal medicine, 1997)
Keywords: Acute Disease; Angioedema - diagnosis; Angioedema - genetics; Angioedema - immunology; Angioedema - mortality; Angioedema - therapy; Biological and medical sciences; C1‐inhibitor deficiency; Chronic Disease; clinical presentation; Complement C1 Inactivator Proteins - deficiency; Complement C4 - metabolism; Dermatology; Diagnosis, Differential; Female; hereditary angiooedema; Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue; Humans; Male; Medical sciences; Pedigree; Pregnancy; Pregnancy Complications, Cardiovascular - etiology; Severity of Illness Index; Human; Immunopathology; Allergy; Symptomatology; Angioneurotic edema; Family study; Evolution; Genetic disease