Selective immunoglobulin A deficiency

Selective immunoglobulin A deficiency (SIgAD) is a genetic disorder in which the body produces little or no Immunoglobulin A (IgA). This is the most common of the primary antibody deficiencies.

Signs and Symptoms

People with SIgAD may appear healthy and symptom-free. However, some people may have frequent infections, particularly of the sinuses, lungs, and gastrointestinal tract. Other symptoms may include allergies, asthma, and autoimmune diseases.

Causes

The exact cause of SIgAD is unknown. It is believed to be a genetic disorder, but the specific genes involved have not been identified. It is also thought that environmental factors may play a role.

Diagnosis

SIgAD is diagnosed through a blood test that measures the level of IgA in the blood. A diagnosis of SIgAD is made when the IgA level is very low or absent, and other causes of low IgA have been ruled out.

Treatment

There is no cure for SIgAD. Treatment is aimed at managing symptoms and preventing infections. This may include antibiotic therapy for infections, immunoglobulin therapy for those with severe symptoms, and vaccination to prevent infections.

See Also

• Immunodeficiency
• Primary immunodeficiency
• Common variable immunodeficiency

References

Selective immunoglobulin A deficiency Resources
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