Self-administered C1 esterase inhibitor concentrates for the management of hereditary angioedema: usability and patient acceptance

Hereditary angioedema (HAE) is a rare genetic disease characterized by episodic subcutaneous or submucosal swelling. The primary cause for the most common form of HAE is a deficiency in functional C1 esterase inhibitor (C1-INH). The swelling caused by HAE can be painful, disfiguring, and life-threat...

Descripción completa

Detalles Bibliográficos
Autor principal: Li, Huamin Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019432/
https://www.ncbi.nlm.nih.gov/pubmed/27660422
http://dx.doi.org/10.2147/PPA.S86379

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019432/
https://www.ncbi.nlm.nih.gov/pubmed/27660422
http://dx.doi.org/10.2147/PPA.S86379

Ejemplares similares