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Advisor(s)
Abstract(s)
Primary immunodeficiency disorders are rarely diagnosed in adults but must be considered in the differential diagnosis of combined recurrent infections and autoimmune disease. We describe a patient with CTLA-4 haploinsufficiency and an abnormal regulatory T-cell phenotype. Unusually, infections were more severe than autoimmunity, illustrating therapeutic challenges in disease course.
Description
Keywords
CTLA‐4 mutation Evans Syndrome Hypogammaglobulinemia Sepsis HCC DAUTOIM
Citation
Send to Clin Case Rep. 2017;5(12):2066-207