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[Familial studies of patients with hereditary angioedema].

Abstract
25 families with 607 members were studied. 165 persons of them suffer from hereditary angioneurotic edema and 28 persons had died from this disease. The clinical forms of the disease are discussed. A classification of angioneurotic edema caused by C-inactivator deficiency is presented. The importance of the examination of C1 inactivator (quantitatively and qualitatively) and of C4 complement fraction in patients with hereditary angioneurotic edema is pointed out.
AuthorsB Bozhkov, K Nikolov, M Baleva
JournalVutreshni bolesti (Vutr Boles) Vol. 27 Issue 4 Pg. 62-5 ( 1988) ISSN: 0506-2772 [Print] Bulgaria
Vernacular TitleFamilni prouchvaniia na bolni ot nasledstven angioedem.
PMID3213025 (Publication Type: Comparative Study, English Abstract, Journal Article)
Chemical References
  • Complement C1 Inactivator Proteins
  • Complement C3
  • Complement C4
Topics
  • Adolescent
  • Adult
  • Angioedema (classification, diagnosis, genetics)
  • Child
  • Complement C1 Inactivator Proteins (blood, deficiency)
  • Complement C3 (analysis)
  • Complement C4 (analysis)
  • Humans
  • Middle Aged

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