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Gennemgang af en ny type hereditært angioødem med normal komplement C1-inhibitor

Forfatter(e)
Maria Bach Okholm-Hansen1, Anna Hillert Winther2, Christina Fagerberg3, Marianne Antonius Jakobsen4 & Anette Bygum2 1) Det Sundhedsvidenskabelige Institut, Syddansk Universitet, Odense 2) Hudafdeling I og Allergicentret, Odense Universitetshospital 3) Klinisk Genetisk Afdeling, Odense Universitetshospital 4) Klinisk Immunologisk Afdeling, Odense Universitetshospital Ugeskr Læger 2018;180:V06170468
Reference: 
Ugeskr Læger 2018;180:V06170468
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Review of a new subtype of hereditary angio-oedema with normal complement C1-inhibitor
Hereditary angio-oedema (HAE) is a rare, potentially fatal disease characterized by recurrent swelling of skin and mucosa. Besides HAE with quantitative (type I) or qualitative (type II) deficiency of complement C1-inhibitor (C1-INH), a new subtype of HAE is now described with normal levels of C1-INH. This subtype is possibly underdiagnosed, and a treatment regimen and general knowledge about the condition is still in its infancy. The purpose of this article is to inform Danish doctors about the disease to identify more Danish patients.
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