These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Selective deficiencies in complement component : a family with hereditary C2 deficiency.
    Author: Dantant M, Rivat C, Gilbert D, Fontaine M, Cavelier B, Godin M, Fillastre JP.
    Journal: Biomedicine; 1978; 28(3):185-90. PubMed ID: 698338.
    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.
    [Abstract] [Full Text] [Related] [New Search]