Hereditary angioedema diagnosis: Reflecting on the past, envisioning the future

Hereditary angioedema diagnosis: Reflecting on the past, envisioning the future

Individuals with hereditary angioedema (HAE), a rare disease most frequently associated with deficiency (HAE-C1INH-Type1) or dysfunction (HAE-C1INH-Type2) of C1 inhibitor (C1INH), continue to experience frequent misdiagnoses and long delays in diagnosis, preventing appropriate management strategies...

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Bibliographic Details
Main Authors: Anete S. Grumach, MD, PhD, Marc A. Riedl, MD, MS, Lei Cheng, MD, PhD, Siddharth Jain, MD, Daniel Nova Estepan, PharmD, RPh, Andrea Zanichelli, MD, PhD
Format: Article
Language:English
Published: Elsevier 2025-06-01
Series:World Allergy Organization Journal
Subjects:
C1 inhibitor
C4
Diagnosis
Genetic testing
Hereditary angioedema
Online Access:http://www.sciencedirect.com/science/article/pii/S1939455125000377
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