Hereditary angioedema: Report of three cases and approach to diagnosis and management Herediter anjiyoödem: Üç olgu sunumu ve tani ve tedavide yaklaşim

Kuş S., Yücelten D.

Turk Dermatoloji Dergisi, cilt.3, sa.2, ss.43-46, 2009 (Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 3 Sayı: 2
  • Basım Tarihi: 2009
  • Dergi Adı: Turk Dermatoloji Dergisi
  • Derginin Tarandığı İndeksler: Scopus
  • Sayfa Sayıları: ss.43-46
  • Anahtar Kelimeler: Antifibrinolytic agent, C1 esterase inhibitor (C1 INH), Complement, Danasole, Hereditary angioedema, Reticular erythema
  • Marmara Üniversitesi Adresli: Evet

Özet

Hereditary angioedema (HAE) is a distinctive form of recurrent angioedema with life threatening consequences. Type I is defined with quantitative C1 esterase inhibitor (C1 INH) deficiency, type II with functional C1 INH deficency and type III with normal quantity and function of C1 INH respectively. Here in, We present three cases with HAE and discuss diagnostic and therapeutic issues.