Demongeot J

ORCID: 0000-0002-8335-9240 · 1 paper in corpus

2024

Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency.

The journal of allergy and clinical immunology. Global ·doi:10.1016/j.jacig.2024.100223

BackgroundHereditary 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…