Flere nye behandlingsmuligheder ved hereditært angioødem

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Abstrakt

Hereditary angio-oedema (HAE) is a rare genetic disease caused by deficiency of complement C1 inhibitor. It is characterised by recurrent episodes of subcutaneous or submucosal oedema typically involving the extremities, bowel, face or larynx. Within the latest years it has become evident that the active mediator of HAE attacks is an increased level of bradykinin and various new treatment modalities have been developed. The aim of this paper is to give an update from the Danish HAE Comprehensive Care Centre on current treatment possibilities and address some of the challenges when diagnosing HAE.
OriginalsprogDansk
TidsskriftUgeskrift for Laeger
Vol/bind174
Udgave nummer34
Sider (fra-til)1894-1898
Antal sider5
ISSN0041-5782
StatusUdgivet - 17. aug. 2012

Emneord

  • Hereditært angioødem

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