A case of hereditary angio-oedema type III presenting with C1-inhibitor cleavage and a missense mutation in the F12 gene

Br J Dermatol. 2007 May;156(5):1063-5. doi: 10.1111/j.1365-2133.2007.07778.x. Epub 2007 Mar 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Angioedema / drug therapy
  • Angioedema / genetics*
  • Antifibrinolytic Agents / therapeutic use
  • Complement C1 Inhibitor Protein / metabolism
  • Female
  • Humans
  • Pregnancy
  • Pregnancy Complications / genetics*
  • Recurrence
  • Tranexamic Acid / therapeutic use

Substances

  • Antifibrinolytic Agents
  • Complement C1 Inhibitor Protein
  • Tranexamic Acid