Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence

BACKGROUND: Hereditary angioedema (HAE) with normal C1 inhibitor (C1-INH) (HAEnCI) is associated with skin swellings, abdominal attacks, and the risk of asphyxia due to upper airway obstruction. Several different gene mutations linked to the HAE phenotype have been identified. Our aim was to qualita...

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Detalles Bibliográficos
Autores principales: Bork, Konrad, Machnig, Thomas, Wulff, Karin, Witzke, Guenther, Prusty, Subhransu, Hardt, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559394/
https://www.ncbi.nlm.nih.gov/pubmed/33059692
http://dx.doi.org/10.1186/s13023-020-01570-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559394/
https://www.ncbi.nlm.nih.gov/pubmed/33059692
http://dx.doi.org/10.1186/s13023-020-01570-x

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