The diagnosis of hereditary angioedema with C1 inhibitor deficiency: a survey of Canadian physicians and laboratories

BACKGROUND: Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is an autosomal dominant disease resulting in random and unpredictable attacks of swelling. The swelling in C1-INH-HAE is a result of impaired regulation of bradykinin production. The fact that the array of tests needed to...

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Detalles Bibliográficos
Autores principales: Charest-Morin, Xavier, Betschel, Stephen, Borici-Mazi, Rozita, Kanani, Amin, Lacuesta, Gina, Rivard, Georges-Étienne, Wagner, Eric, Wasserman, Susan, Yang, Bill, Drouet, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249925/
https://www.ncbi.nlm.nih.gov/pubmed/30479631
http://dx.doi.org/10.1186/s13223-018-0307-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249925/
https://www.ncbi.nlm.nih.gov/pubmed/30479631
http://dx.doi.org/10.1186/s13223-018-0307-0

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