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...

Descripción completa

Detalles Bibliográficos
Autores principales: Grivcheva-Panovska, Vesna, Giannetti, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
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

Internet

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

Ejemplares similares