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- W1966602009 abstract "<h3>Background</h3> Common variable immunodeficiency (CVID), a diverse immunodeficiency syndrome characterized by low immunoglobulin levels and recurrent infections, has been observed in families with the HLA A1 B8 DR3 haplotype. <h3>Methods</h3> We report a two-generation family with three members affected by CVID. Immunoglobulin levels, antibody titers, lymphocyte marker analyses, T cell proliferation assays, and HLA typing were performed on the affected family members. <h3>Results</h3> Studies of the affected patients revealed low levels of immunoglobulin G and A; normal tetanus, rubella and rubeola antibody titers; low B cell numbers; normal T cell numbers; normal CD4/CD8 ratios and normal lymphocyte proliferation studies. HLA typing did not reveal the HLA A1 B8 DR3 haplotype previously associated with familial CVID. <h3>Conclusion</h3> We report a family with a unique presentation of CVID involving possible genetic inheritance other than the HLA A1 B8 DR3 haplotype and possessing lymphocyte characteristics distinct from those usually seen in sporadic CVID." @default.
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- W1966602009 date "1996-06-01" @default.
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- W1966602009 title "Analysis of a Family Containing Three Members with Common Variable Immunodeficiency" @default.
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- W1966602009 doi "https://doi.org/10.1016/s1081-1206(10)63272-3" @default.
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