Pediatric hereditary angioedema: an update

F1000Res. 2017 Jul 24:6:F1000 Faculty Rev-1205. doi: 10.12688/f1000research.11320.1. eCollection 2017.

Abstract

Hereditary angioedema (HAE) with C1-inhibitor (C1-Inh) deficiency (C1-Inh-HAE) is a rare, life-threatening, and disabling genetic disorder characterized by self-limited tissue swelling caused by deficiency or dysfunction of C1-Inh. Our aim in this update is to discuss new advances in HAE therapy, focusing mainly on the various treatment options that have become available recently and also drugs that are under trial for prophylaxis to prevent attacks. There is a paradigm shift to where the treatment of HAE is headed, focusing now on prophylactic treatment rather than abortive management.

Keywords: C1-INH gene; Genetic disorder; HAE; Hereditary angioedema.

Publication types

  • Review

Grants and funding

The author(s) declared that no grants were involved in supporting this work.