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Considerations in the management of hereditary angioedema due to C1-INH deficiency in women of childbearing age
Hereditary angioedema (HAE) is a rare, autosomal disorder that manifests with unpredictable episodes of severe swelling of the skin and mucous membranes. These attacks can be highly disfiguring and range in severity from mild to—in cases of airway swelling—life-threatening. Fluctuations in female se...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9281160/ https://www.ncbi.nlm.nih.gov/pubmed/35831891 http://dx.doi.org/10.1186/s13223-022-00689-9 |