| Literature DB >> 27071490 |
Bruce L Zuraw1,2, Sandra C Christiansen1.
Abstract
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder clinically characterized by recurrent attacks of subcutaneous and mucosal swelling that can result in significant morbidity and even mortality. Several novel therapies introduced since 2008 have dramatically transformed the approach to management. In this review we will discuss the current understanding of the pathophysiology of HAE, diagnostic evaluation of recurrent angioedema without urticaria, and the therapeutic approach to HAE. We advocate taking an integrative approach to care in order to normalize the lives of affected patients.Entities:
Keywords: C1 inhibitor; Hereditary angioedema; Management; bradykinin; treatment
Mesh:
Year: 2016 PMID: 27071490 DOI: 10.1111/bjh.14059
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998