A Case Report of Hereditary Angioedema: Challenges in Diagnosis and Management
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder which causes bradykinin mediated angioedema. Although it can be life threatening, HAE may be underdiagnosed due to a lack of awareness of the disease and limited access to laboratory testing. Here, we report a case of HAE whi...
Saved in:
Main Authors: | Alvina Widhani, Suzy Maria, Rifky Yulian, Anshari Saifuddin Hasibuan, Sukamto Koesnoe |
---|---|
Format: | Article |
Language: | English |
Published: |
Interna Publishing
2023-07-01
|
Series: | Acta Medica Indonesiana |
Subjects: | |
Online Access: | http://www.actamedindones.org/index.php/ijim/article/view/2217 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
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) -
Global frequency, diagnosis, and treatment of hereditary angioedema with normal C1 inhibitor
by: Markus Magerl, MD, et al.
Published: (2025-08-01)