Screening for type II hereditary angioedema—the “poor man’s c1-inhibitor function”

Screening for type II hereditary angioedema—the “poor man’s c1-inhibitor function”

Background: Hereditary angioedema (HAE) is a rare genetic disease. Patients with type II HAE have normal or elevated C1-inhibitor (C1-INH) levels but C1-INH protein is dysfunctional. C1-INH function requires careful sample handling and technical expertise and may account for the lack of diagnosed pa...

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Bibliographic Details
Main Authors: Ankur Kumar Jindal, MD, DM, Valerie Chiang, MBBS, Prabal Barman, MD, Archan Sil, MD, Sanchi Chawla, MSc, Elaine Y.L. Au, MBBS, FRCPA, Amit Rawat, MD, Philip H. Li, MD, FRCP
Format: Article
Language:English
Published: Elsevier 2024-02-01
Series:Journal of Allergy and Clinical Immunology: Global
Subjects:
C1 inhibitor
hereditary angioedema
function
level
screening
type 2 HAE
Online Access:http://www.sciencedirect.com/science/article/pii/S2772829323001042

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http://www.sciencedirect.com/science/article/pii/S2772829323001042

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