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Improving patient outcomes in hereditary angioedema: reducing attack frequency using routine prevention with C1 inhibitor concentrate

Hereditary angioedema (HAE) is a rare inherited disorder, characterised by recurrent oedema attacks in various regions of the body. In HAE, mutations in the C1 esterase inhibitor (C1-INH) gene result in decreased C1-INH concentrations (type I HAE) or functionally deficient C1-INH (type II HAE), lead...

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Bibliografiske detaljer
Main Authors: Dominas, Nina, Hoffmann, Thomas K, Bas, Murat, Greve, Jens
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Publishing Group 2014
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4039800/
https://ncbi.nlm.nih.gov/pubmed/24850548
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-200873
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