QR code

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency

Background: Hereditary angioedema (HAE) is a potentially life-threatening disorder characterized by recurrent episodes of subcutaneous or submucosal swelling. HAE with normal C1 inhibitor (HAE-nC1-INH) is an underdiagnosed condition. Although the association with genetic variants has been identified...

Volledige beschrijving

Bewaard in:
Hoofdauteurs: Denis Vincent, MD, PhD, Faidra Parsopoulou, PharmD, PhD, Ludovic Martin, MD, PhD, Christine Gaboriaud, PhD, Jacques Demongeot, MD, PhD, Gedeon Loules, MSc, Sascha Fischer, MSc, Sven Cichon, PhD, Anastasios E. Germenis, MD, PhD, Arije Ghannam, MD, PhD, Christian Drouet, PharmD, PhD
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Elsevier 2024-05-01
Reeks:Journal of Allergy and Clinical Immunology: Global
Onderwerpen:
Urticaria
angioedema
hereditary carboxypeptidase N deficiency
CPN1 gene
Online toegang:http://www.sciencedirect.com/science/article/pii/S2772829324000195
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items