Literature DB >> 3490240

[Hereditary deficiency of the 4th component of complement (C4) associated with a lupic syndrome].

R Dumas, G Hauptmann, E Chayon, S Bascoul, A Serre, P Baldet, A Naoumis.   

Abstract

A 2 year-old girl presented with bacterial meningitis followed by a lupus erythematosus syndrome consisting of erythematous rash, Raynaud's phenomenon and mutilating cicatricia atrophy; high speckled antinuclear antibodies and anti-Sm and anti-Ro antibodies titers; a selective absence of C4; moderate mesangial proliferation with IgM and C1q mesangial deposits. Study of the family revealed a linkage of C4 deficiency with the HLA A1 B17/BfF haplotype.

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Year:  1986        PMID: 3490240

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  2 in total

1.  Molecular basis of complete complement C4 deficiency in two North-African families with systemic lupus erythematosus.

Authors:  Y L Wu; G Hauptmann; M Viguier; C Y Yu
Journal:  Genes Immun       Date:  2009-03-12       Impact factor: 2.676

2.  Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family.

Authors:  V Fremeaux-Bacchi; B Uring-Lambert; L Weiss; P Brun; J Blouin; D Hartmann; C Loirat; G Hauptmann; M D Kazatchkine
Journal:  J Clin Immunol       Date:  1994-09       Impact factor: 8.317

  2 in total

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