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What is Advances in Hereditary Angioedema Treatment about?

Hereditary angioedema (HAE) is a rare genetic disorder caused by a deficiency in C1 inhibitor (C1 INH) protein, which regulates the complement, contact, and coagulation systems. This deficiency leads to uncontrolled activation of bradykinin and symptoms of pain, swelling, and edema, most often affecting the skin, face, intestinal tract, and airway. New treatments have been developed that target components of the contact system like plasma kallikrein inhibitor and bradykinin B2 receptor antagonist. This revi

Author

Laura Sofia

Language

EN