Case report: Recurrent angioedema: Diagnosing the rare and the frequent

Case report: Recurrent angioedema: Diagnosing the rare and the frequent

Hereditary angiodema with normal C1 inhibitor and unknown mutation (HAE-nC1INH-UNK), an exceedingly rare subtype of HAE, appears to be often diagnosed in patients who do not have this condition, but have mast cell-mediated angioedema. Here, we report two patients diagnosed with HAE-nC1INH-UNK by the...

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Bibliographic Details
Main Authors: Thomas Buttgereit, Lauré M. Fijen, Carolina Vera, Karl-Christian Bergmann, Marcus Maurer, Markus Magerl
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Frontiers in Medicine
Subjects:
angioedema
recurrent
mast cell
omalizumab
normal C1INH
HAE
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2022.1048480/full

Internet

https://www.frontiersin.org/articles/10.3389/fmed.2022.1048480/full

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