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Treatment of Hereditary Angioedema with Lanadelumab: Four Case Reports and Literature Review

Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder characterized by recurrent episodes of subcutaneous and submucosal edema, which can be life-threatening in severe cases. Lanadelumab, a recombinant human monoclonal antibody against kallikrein, has been recommended as a first-...

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Main Authors: ZHANG Wenjing, CAI Liping, LIU Yun, LAI He
Format: Artigo
Jezik:Chinês
Izdano: Editorial Office of Journal of Rare Diseases 2025-07-01
Serija:罕见病研究
Teme:
Online dostop:https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2025.03.007
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