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Review
. 2000 May;120(2):225-31.
doi: 10.1046/j.1365-2249.2000.01131.x.

Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)

L Hammarström  1 , I Vorechovsky, D Webster
Affiliations
Review

Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)

L Hammarström et al. Clin Exp Immunol. 2000 May.
No abstract available

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Figures

Fig. 1
Fig. 1
Three pedigrees are shown demonstrating the inheritance patterns for IgAD and CVID. Note that in some families there are relatives with minor IgG abnormalities.
See this image and copyright information in PMC

References

    1. Primary Immunodeficiency Diseases. Report of a WHO Scientific Group WHO. Clin Exp Immunol. 1997;159:6236–41. - PubMed
    1. Hammarström L, Smith CIE. Genetic approach to common variable immunodeficiency and IgA deficiency. In: Ochs H, Smith CIE, Puck J, Smith CIE, editors. Primary immunodeficiency diseases, a molecular and genetic approach. Oxford: Oxford University Press; 1999. pp. 250–62.
    1. Hammarström L, Persson MAA, Smith CIE. Immunoglobulin subclass distribution of human anti-carbohydrate antibodies: aberrant pattern in IgA deficient donors. Immunology. 1985;54:821–6. - PMC - PubMed
    1. Oxelius V-A, Laurell AB, Lindqvist B, Henryka G, Axelsson U, Björkander J, Hanson L-Å. IgG subclasses in selective IgA deficiency. Importance of IgG2-IgA deficiency. N Engl J Med. 1981;304:1476–7. - PubMed
    1. Hammarström L, Grubb R, Jakobsen BK, Oxelius V, Persson U, Smith CIE. Concomitant deficiency of IgG4 and IgE in IgA deficient donors with high titres of anti-IgA. Monogr Allergy. 1986;20:234–5.

MeSH terms