Cargando…
Malignancy and immune disorders in patients with hereditary angioedema
BACKGROUND: Hereditary angioedema (HAE) is an inherited condition manifesting as recurrent angioedema episodes which is caused by deficiency or dysfunction of C1 inhibitor. Although complement dysregulation has historically been shown to be associated with various malignancy and immune disorders, it...
Autores principales: | Stepaniuk, Peter, Kanani, Amin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684618/ https://www.ncbi.nlm.nih.gov/pubmed/34924008 http://dx.doi.org/10.1186/s13223-021-00621-7 |
Ejemplares similares
-
The role of C1 inhibitor and complement as acute phase reactants: are we missing the diagnosis of hereditary angioedema?
por: Stepaniuk, Peter, et al.
Publicado: (2021) -
Selective cannabis strain allergy in a patient presenting with a local allergic reaction
por: Stepaniuk, Peter, et al.
Publicado: (2021) -
Anaesthetic Approach for Patient with Hereditary Angioedema
por: Melo, Maize Cordeiro, et al.
Publicado: (2020) -
Hereditary Angioedema: Not An Allergy
por: Bhivgade, Sanjay, et al.
Publicado: (2012) -
Impact of lanadelumab in hereditary angioedema: a case series of 12 patients in Canada
por: Iaboni, Aled, et al.
Publicado: (2021)