首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis.
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Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis.

机译:家族性类风湿关节炎:HLA与四个先证者患有幼年类风湿关节炎的家庭的疾病易感性位点相关。

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摘要

The occurrence of a chronic seronegative polyarthritis has been studied in four families in which the proband presented with some form of juvenile rheumatoid arthritis. In these families, histocompatibility testing suggested that susceptibility to arthritis was controlled by a dominant allele with variable penetrance and expressivity at the rheumatoid-like arthritis, first locus (RLA-1). The combined lod scores for the four families (2.70) indicated that the odds in favor of genetic linkage between the major histocompatibility complex and the postulated disease susceptibility gene, RLA-1, were 500:1. In one family, a recombinant event permitted localization of RLA-1 centromeric to HLA-D. Of major interest was the fact that there was significant pleomorphism in the clinical manifestations of arthritis in affected individuals. In some, symptoms first occurred in childhood and in others, in adult life. Even among those with childhood-onset arthritis, different types of juvenile rheumatoid arthritis were observed within the same family.
机译:已经在四个家族中研究了慢性血清阴性多发性关节炎的发生,其中先证者患有某种形式的青少年类风湿性关节炎。在这些家族中,组织相容性测试表明,关节炎的易感性由类风湿样关节炎的第一个基因位点(RLA-1)的显性和显性变化的显性等位基因控制。四个家族的总lod得分(2.70)表明,主要组织相容性复合体与假定的疾病易感性基因RLA-1之间建立遗传连锁的几率是500:1。在一个家族中,重组事件使得RLA-1着丝粒定位于HLA-D。最令人感兴趣的是,在受影响的个体中,关节炎的临床表现存在明显的多态性。在某些情况下,症状首先发生在儿童时期,而另一些情况则发生在成年生活中。即使在患有儿童期关节炎的人中,在同一家庭中也观察到不同类型的青少年类风湿关节炎。

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