Bruton's agammaglobulinemia; X-linked agammaglobulinemia
The person may have a family history of agammaglobulinemia (or other immune disorder).
Symptoms include frequent episodes of:
Infections typically appear in the first 4 years of life.
The disorder is confirmed by laboratory measurement of blood immunoglobulins. Tests include:
Azar AE. Evaluation of the adult with suspected immunodificiency. Am J Med. 2007;120(9):764-8.
Bonilla FA. Update on primary immunodeficiency diseases. J Allergy Clin Immunol. 2006;117(2 Suppl Mini-Primer):S435-41.
Morimoto Y. Immunodeficiency overview. Prim Care. 2008;35(1):159-73,viii.