C1 inhibitor deficient hereditary angioedema is related to endothelial dysfunction in young adult and middle‐aged patients

C1 inhibitor deficient hereditary angioedema is related to endothelial dysfunction in young adult and middle‐aged patients

Abstract Background Hereditary angioedema (HAE) is a rare, autosomal dominantly inherited disease characterised by mucocutaneous oedema attacks. Vasoactive mediators and the endothelium play an important role in the pathogenesis of HAE. We aimed to evaluate the endothelial dysfunction in HAE. Method...

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Bibliographic Details
Main Authors: Gokce Gul Atay Sensoy, Derya Baykız, İlkim Deniz Toprak, Deniz Eyice Karabacak, Erdem Bektas, Derya Unal, Aslı Gelincik, Semra Demir
Format: Article
Language:English
Published: Wiley 2025-06-01
Series:Clinical and Translational Allergy
Subjects:
carotid intima‐media thickness
endothelial dysfunction
flow‐mediated dilation
hereditary angioedema
Online Access:https://doi.org/10.1002/clt2.70076
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https://doi.org/10.1002/clt2.70076

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