Global frequency, diagnosis, and treatment of hereditary angioedema with normal C1 inhibitor

Background: Hereditary angioedema (HAE) is a rare genetic disease, most frequently associated with deficiency or dysfunction in the C1 inhibitor protein. HAE with normal C1 inhibitor (HAE-nC1INH) lacks standardized diagnostic tests, limiting precise prevalence estimates and development of specific t...

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Principais autores:	Markus Magerl, MD, Marc A. Riedl, MD, MS, Luisa Karla Arruda, MD, PhD, Andrea Bauer, MD, MPH, Alejandro Berardi, MD, Jonathan A. Bernstein, MD, Laurence Bouillet, MD, PhD, Matthew Buckland, PhD, Thomas Buttgereit, MD, Danny M. Cohn, MD, PhD, Timothy Craig, DO, Roberta F. Criado, MD, PhD, Aurélie Du-Thanh, MD, PhD, Olivier Fain, MD, Margarida Gonçalo, MD, PhD, Jens Greve, MD, Anete Sevciovic Grumach, MD, PhD, Mar Guilarte, MD, PhD, Constance Katelaris, MD, PhD, Tamar Kinaciyan, MD, Elena A. Latysheva, MD, Ramon Lleonart, MD, Oscar Calderón Llosa, MD, Eli Mansour, MD, PhD, Vesna Grivcheva-Panovska, MD, PhD, Claudio Parisi, MD, Nelson Augusto Rosario Filho, MD, PhD, Amélia Spínola Santos, MD, Petra Staubach, MD, Anna Valerieva, MD, PhD, Solange Oliveira Rodrigues Valle, MD, PhD, Sherry Danese, MBA, Julie Ulloa, Paul K. Audhya, MD, MBA, Marcus Maurer, MD
Format:	Artigo
Jezik:	Inglês
Izdano:	Elsevier 2025-08-01
Serija:	Journal of Allergy and Clinical Immunology: Global
Teme:	Hereditary angioedema normal C1INH prevalence diagnostics treatment management
Online dostop:	http://www.sciencedirect.com/science/article/pii/S2772829325000475
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