selective IgA deficiency

abbrev: SIgAD
https://doi.org/10.1351/goldbook.13668
Most common form of primary immunodeficiency.
Note: Autoimmunity is the most prevalent manifestation of this deficiency. Individuals with SIgAD have an increased risk of developing systemic [e.g., systemic lupus erythematosus (SLE), rheumatoid arthritis (RA)] and organ-specific (e.g., celiac disease) autoimmune disorders.
Source:
PAC, 2012, 84, 1113. (IUPAC glossary of terms used in immunotoxicology (IUPAC Recommendations 2012)) on page 1243 [Terms] [Paper]
Citation: 'selective IgA deficiency' in IUPAC Compendium of Chemical Terminology, 5th ed. International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. https://doi.org/10.1351/goldbook.13668 RIS BibTex EndNote
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