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Hereditary Angioedema Attack in Utero and Treatment of the Mother and Fetus
Hereditary angioedema (HAE), an inherited deficiency of functional C1 esterase inhibitor (C1-INH), is characterized by unpredictable recurrent episodes of painful and often disabling swelling in subcutaneous and/or submucosal tissues. We report the case of a 23-year-old woman with type I HAE who had...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557207/ https://www.ncbi.nlm.nih.gov/pubmed/33083708 http://dx.doi.org/10.1016/j.mayocpiqo.2020.06.004 |