Recent developments in the treatment of acute abdominal and facial attacks of hereditary angioedema: focus on human C1 esterase inhibitor

Hereditary angioedema (HAE) is a potentially fatal genetic disorder typified by a deficiency (type I) or dysfunction (type II) of the C1-inhibitor (C1-INH) and characterized by swelling of the extremities, face, trunk, abdominal viscera, and upper airway. Type III is normal estrogen-sensitive C1-INH...

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Detalles Bibliográficos
Autores principales: Cardona, Lourdes Pastó, Bellfill, Ramon Lleonart, Caus, Joaquim Marcoval
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681170/
https://www.ncbi.nlm.nih.gov/pubmed/23776358
http://dx.doi.org/10.2147/TACG.S9275

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681170/
https://www.ncbi.nlm.nih.gov/pubmed/23776358
http://dx.doi.org/10.2147/TACG.S9275

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