Successful use of daily intravenous infusion of C1 esterase inhibitor concentrate in the treatment of a hereditary angioedema patient with ascites, hypovolemic shock, sepsis, renal and respiratory failure

Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonly associated with defects in C1 esterase inhibitor (C1-INH). HAE manifests as recurrent episodes of edema in various body locations. Atypical symptoms, such as ascites, acute respiratory distress syndrome, and hypovolemic s...

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Detalles Bibliográficos
Autores principales: Pham, Hoang, Santucci, Stephanie, Yang, William H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268856/
https://www.ncbi.nlm.nih.gov/pubmed/25520740
http://dx.doi.org/10.1186/s13223-014-0062-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268856/
https://www.ncbi.nlm.nih.gov/pubmed/25520740
http://dx.doi.org/10.1186/s13223-014-0062-9

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