Literature DB >> 698338

Selective deficiencies in complement component : a family with hereditary C2 deficiency.

M Dantant, C Rivat, D Gilbert, M Fontaine, B Cavelier, M Godin, J P Fillastre.   

Abstract

We report herein a new case of C2 deficiency in a patient with systemic lupus. The subject and one of her brothers, who shows no clinical manifestations, are hymozygous C2 deficient. All other family members are heterozygous for the C2 deficiency. Gene for C2 deficiency (C2d) was shown to be inherited with HLA-A9, B7/Bfs and HLA-A10, B27/Bfs haplotypes. This association has not previously been described.

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Year:  1978        PMID: 698338

Source DB:  PubMed          Journal:  Biomedicine        ISSN: 0300-0893


  3 in total

Review 1.  Lupus diseases associated with hereditary and acquired deficiencies of complement.

Authors:  V Agnello
Journal:  Springer Semin Immunopathol       Date:  1986

2.  Deficiency of the second complement component association with the HLA haplotype A10, B18 in a normal population.

Authors:  R I Rynes; A F Britten; R J Pickering
Journal:  Ann Rheum Dis       Date:  1982-02       Impact factor: 19.103

Review 3.  The complement system and adverse pregnancy outcomes.

Authors:  Jean F Regal; Jeffrey S Gilbert; Richard M Burwick
Journal:  Mol Immunol       Date:  2015-03-21       Impact factor: 4.407

  3 in total

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