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[Familial lupus erythematosus with partial C4 deficiency].

作者信息

Ploier R, Tappeiner G, Spaeth P, Emhofer J

机构信息

Kinderabteilung des Landeskrankenhauses Steyr.

出版信息

Wien Klin Wochenschr. 1993;105(11):323-6.

PMID:8333199
Abstract

A report is presented of a family with selective partial C4-deficiency in 3 members, two of whom suffer from systemic lupus erythematosus (SLE). C4-allotyping showed the presence of one "silent gene" for the C4B-locus (C4BQO) in these three cases. Presumably it is not the reduced C4-content per se that plays the essential role in the pathogenesis of familial SLE, but the combination of the C4BQO-allele with the HLA-DR2, which was also present in all three affected persons. However, it is of practical relevance that strikingly low C4-levels in comparison with the C3-levels in patients with early onset of SLE should initiate an investigation of the whole family. Furthermore, the C4-level in this form of familial SLE is not a suitable parameter for ganging disease activity on follow-up control investigations.

摘要

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