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Vitiligo and dysgammaglobulinemia. A case report and family study.

Abstract

This report concerns an 8 year old female with vitiligo and dysgammaglobulinemia characterized by absent IgA, very low IgG, and normal IgM. The t-cell immune system was intact but other family members had low levels or absence of IgA. The possible relationship of dysgammaglobulinemia and vitiligo is discussed along with the classification and inheritance of the immune cell defects.

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  • Publisher Full Text
  • Authors

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    Source

    Clinical genetics 7:1 1975 Jan pg 62-76

    MeSH

    Adolescent
    Adult
    Age Determination by Skeleton
    Aged
    Biopsy
    Child
    Child, Preschool
    Dysgammaglobulinemia
    Female
    Humans
    Immunity, Cellular
    Immunoglobulin A
    Immunoglobulin G
    Immunoglobulin M
    Immunologic Deficiency Syndromes
    Indiana
    Lymph Nodes
    Male
    Pedigree
    Skin
    Vitiligo

    Pub Type(s)

    Journal Article

    Language

    eng

    PubMed ID

    163713

    Citation

    Bader, P I., et al. "Vitiligo and Dysgammaglobulinemia. a Case Report and Family Study." Clinical Genetics, vol. 7, no. 1, 1975, pp. 62-76.
    Bader PI, Biegel A, Epinette WW, et al. Vitiligo and dysgammaglobulinemia. A case report and family study. Clin Genet. 1975;7(1):62-76.
    Bader, P. I., Biegel, A., Epinette, W. W., & Nance, W. E. (1975). Vitiligo and dysgammaglobulinemia. A case report and family study. Clinical Genetics, 7(1), pp. 62-76.
    Bader PI, et al. Vitiligo and Dysgammaglobulinemia. a Case Report and Family Study. Clin Genet. 1975;7(1):62-76. PubMed PMID: 163713.
    * Article titles in AMA citation format should be in sentence-case
    TY - JOUR T1 - Vitiligo and dysgammaglobulinemia. A case report and family study. AU - Bader,P I, AU - Biegel,A, AU - Epinette,W W, AU - Nance,W E, PY - 1975/1/1/pubmed PY - 1975/1/1/medline PY - 1975/1/1/entrez SP - 62 EP - 76 JF - Clinical genetics JO - Clin. Genet. VL - 7 IS - 1 N2 - This report concerns an 8 year old female with vitiligo and dysgammaglobulinemia characterized by absent IgA, very low IgG, and normal IgM. The t-cell immune system was intact but other family members had low levels or absence of IgA. The possible relationship of dysgammaglobulinemia and vitiligo is discussed along with the classification and inheritance of the immune cell defects. SN - 0009-9163 UR - https://www.unboundmedicine.com/medline/citation/163713/Vitiligo_and_dysgammaglobulinemia__A_case_report_and_family_study_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0009-9163&date=1975&volume=7&issue=1&spage=62 DB - PRIME DP - Unbound Medicine ER -