The cause of the syndrome is unknown. It is related to IgG subclass deficiencies and there is a failure to respond to specific antigens. This entity, observed more in adults, clinically resembles common variable immunodeficiency (CVI). In small children, it is due to a maturational delay that resolves spontaneously.
Alternative names
Antibody deficiency with normal or elevated serum immunoglobulin levels
Selective antibody deficiency with normal immunoglobulins
Classification
- Deficiencies predominantly affecting antibody production
- Other antibody deficiencies
Inheritance
Unknown
OMIM
%240500 Common variable immunodeficiency
Cross references
Phenotypically related immunodeficiencies
Incidence
Incidence is not known.