Selective IgA deficiency disease

A dysgammaglobulinemia characterized by low or undetectable serum levels of immunoglobulin class A (IgA). It is the most common primary antibody deficiency. It may be inherited or the reversible sequela of infection or certain drugs. It may be caused by decreased or inefficient class-switching from progenitor B cells without any corresponding decreases in the other isotypes. Though affected persons may be asymptomatic, low levels of IgA will reduce the immune system's ability to combat infection where IgA is normally secreted, at mucosal surfaces. Selective IgA deficiency is seen in greater proportion among patients with autoimmune disorders.

Also known as: SIgAD, immunoglobulin A deficiency, selective IgA immunodeficiency, IgA deficiencies, deficiencies, IgA, deficiency, IgA, immunoglobulin alpha deficiency

43 clinical trials for this condition and its sub-types, 2 tagged with Selective IgA deficiency disease itself.