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agammaglobulinemia type 2
Pathology:
- primary immunodeficiency
- early block of B-cell development
Genetics:
- associated with defects in IGLL1
Clinical manifestations:
- severe infections in the first years of life
Laboratory:
- low or absent serum antibodies (serum IgG) (serum IgM)
- & low B-cell count in blood
General
agammaglobulinemia
genetic disease of the immune system
Database Correlations
OMIM 613500
References
OMIM :accession 613500