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...
Saved in:
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: | |
Online Access: | https://doi.org/10.1002/clt2.70076 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management
by: Alvina Widhani, et al.
Published: (2023-07-01) -
Exercise-Induced Angioedema, Urticaria, and Anaphylaxis—A Narrative Review
by: Waleed Aman Ur Rahman, et al.
Published: (2025-07-01) -
Disease control and disease activity in hereditary angioedema: two sides of the same coin?
by: Behzad Heibati, et al.
Published: (2025-07-01) -
Bradykinin measurement by liquid chromatography tandem mass spectrometry in subjects with hereditary angioedema enhanced by cold activation
by: Jinguo Chen, MD, et al.
Published: (2025-08-01) -
Successful long-term prophylaxis of hereditary pregnancy-associated angioedema with plasma-derived C1-inhibitor concentrate: a case report
by: D. V. Demina, et al.
Published: (2021-01-01)