Complement Study Versus CINH Gene Testing for the Diagnosis of Type I Hereditary Angioedema in Children

J Clin Immunol. 2016 Jan;36(1):16-8. doi: 10.1007/s10875-015-0222-9. Epub 2015 Dec 10.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Bradykinin / metabolism
  • Child
  • Child, Preschool
  • Complement Activation / genetics
  • Complement C1 Inactivator Proteins / genetics
  • Complement C1 Inactivator Proteins / metabolism*
  • Complement C1 Inhibitor Protein
  • DNA Mutational Analysis
  • Early Diagnosis
  • Female
  • Hereditary Angioedema Types I and II / diagnosis*
  • Humans
  • Infant
  • Male
  • Mutation / genetics
  • Pedigree

Substances

  • Complement C1 Inactivator Proteins
  • Complement C1 Inhibitor Protein
  • SERPING1 protein, human
  • Bradykinin