Therapeutic trial in hereditary angioedema type III: Icatibant

نویسندگان

  • Laila Sabino Garro
  • Maria Helena Mattos Porter
  • Fernanda Komaroff
  • Caroline Terumi Adachi
  • Maria Teresinha Malheiros
  • Yara Mello
  • Marisa Rosimeire Ribeiro
چکیده

Background Hereditary angioedema (HAE) is a disease transmitted by autosomal dominant inheritance, characterized by quantitative and / or functional deficiency of C1 inhibitor (C1-INH), which causes episodes of swelling, with involvement of many organs. HAE is currently divided into three groups. The HAE type III is a less frequent disorder that mainly affects women and is characterized by normal levels and activity of C1-INH.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2015