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...

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Detalles Bibliográficos
Autores principales: Hsu, Florence Ida, Lumry, William, Riedl, Marc, Tachdjian, Raffi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
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

Internet

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

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