Co-occurrence between C1 esterase inhibitor deficiency and autoimmune disease: a systematic literature review

BACKGROUND: Hereditary angioedema (HAE) is caused by a SERPING1 gene defect resulting in decreased (Type I) or dysfunctional (Type II) C1 esterase inhibitor (C1-INH). The prevalence of autoimmune diseases (ADs) in patients with HAE appears to be higher than the general population. A systematic liter...

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Detalles Bibliográficos
Autores principales: Levy, Donald, Craig, Timothy, Keith, Paul K., Krishnarajah, Girishanthy, Beckerman, Rachel, Prusty, Subhransu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254644/
https://www.ncbi.nlm.nih.gov/pubmed/32514272
http://dx.doi.org/10.1186/s13223-020-00437-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254644/
https://www.ncbi.nlm.nih.gov/pubmed/32514272
http://dx.doi.org/10.1186/s13223-020-00437-x

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