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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