Clinical Experience with Berotralstat in Patients with Hereditary Angioedema with Normal C1-Esterase Inhibitor: A Commented Case Series
Hereditary angioedema (HAE) is a rare genetic disorder characterized by potentially life-threatening episodes of swelling. Most HAE cases are caused by deficient (type I) or dysfunctional (type II) C1-esterase inhibitor (C1-INH) protein. However, some patients present with a subtype of HAE that is a...
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Veröffentlicht in: | Journal of asthma and allergy 2024, Vol.17, p.123-132 |
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Hauptverfasser: | , |
Format: | Report |
Sprache: | eng |
Online-Zugang: | Volltext |
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