The official journal of CSACI
Co-occurrence between C1 esterase inhibitor deficiency and autoimmune disease: a systematic literature review
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 patient...
Citation: Allergy, Asthma & Clinical Immunology 2020 16:41