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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Detalles Bibliográficos
Autores principales: Buttgereit, Thomas, Fijen, Lauré M., Vera, Carolina, Bergmann, Karl-Christian, Maurer, Marcus, Magerl, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756157/
https://www.ncbi.nlm.nih.gov/pubmed/36530887
http://dx.doi.org/10.3389/fmed.2022.1048480

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756157/
https://www.ncbi.nlm.nih.gov/pubmed/36530887
http://dx.doi.org/10.3389/fmed.2022.1048480

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