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...

Source: Allergy, Asthma and Clinical Immunology - May 27, 2020 Category: Allergy & Immunology Authors: Donald Levy, Timothy Craig, Paul K. Keith, Girishanthy Krishnarajah, Rachel Beckerman and Subhransu Prusty Tags: Research Source Type: research