Biochemistry, molecular genetics, and clinical aspects of hereditary angioedema with and without C1 inhibitor deficiency
Hereditary angioedema (HAE) is a rare disorder characterized by cutaneous and submucosal swelling caused mostly by excessive local bradykinin production. Bradykinin is a vasoactive peptide generated by the limited proteolysis of high molecular weight kininogen (HMWK) by plasma kallikrein via the con...
Main Authors: | Toshiyuki Miyata, Takahiko Horiuchi |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2023-07-01
|
Series: | Allergology International |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1323893023000424 |
Similar Items
-
Clinical Characteristics and Management of Angioedema Attacks in Polish Adult Patients with Hereditary Angioedema Due to C1-Inhibitor Deficiency
by: Katarzyna Piotrowicz-Wójcik, et al.
Published: (2021-11-01) -
Current and Future Therapy of Hereditary Angioedema
by: Öner Özdemir
Published: (2020-10-01) -
Abdominal and pelvic imaging in the diagnosis of acute abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency
by: Piotr Obtułowicz, et al.
Published: (2021-08-01) -
Pediatric Angioedema without Wheals: How to Guide the Diagnosis
by: Lucia Liotti, et al.
Published: (2023-04-01) -
The Role of Bradykinin Receptors in Hereditary Angioedema Due to C1-Inhibitor Deficiency
by: Wojciech Dyga, et al.
Published: (2022-09-01)