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澳大利亚人群中的特发性血色素沉着症:HLA连锁与隐性遗传

Idiopathic haemochromatosis in the Australian population: HLA linkage and recessivity.

作者信息

Doran T J, Bashir H V, Trejaut J, Bassett M L, Halliday J W, Powell L W

出版信息

Hum Immunol. 1981 May;2(3):191-200. doi: 10.1016/0198-8859(81)90011-2.

Abstract

Studies of 78 unrelated patients and 19 families with idiopathic haemochromatosis are reported. The unrelated patients showed a highly significant association between the disease and HLA-A3. There was a less strong association with HLA-B7 and HLA-DRw2 attributed to the linkage disequilibrium between HLA-A3, B7, and DRw2. Lod scores and haplotype analysis of the families indicated a recessive mode of inheritance for an idiopathic haemochromatosis susceptibility factor in close linkage with the HLA region. These results, for Australian caucasoid patients, are not in total agreement with those reported in studies of other populations.

摘要

报告了对78例非亲属特发性血色素沉着症患者及19个家族的研究。非亲属患者显示出该疾病与HLA - A3之间存在高度显著的关联。与HLA - B7和HLA - DRw2的关联较弱,这归因于HLA - A3、B7和DRw2之间的连锁不平衡。对家族的连锁分析分数和单倍型分析表明,特发性血色素沉着症易感性因子以隐性方式遗传,且与HLA区域紧密连锁。对于澳大利亚白种人患者,这些结果与其他人群研究中报告的结果并不完全一致。

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