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选择性IgA缺乏症与HLA - B8抗原。两例家族数据报告。

Selective IgA deficiency and the HLA-B8 antigen. Report of two cases with familial data.

作者信息

Perez-Jimenez F, Lopez P B, Tallo E P, Guzman J R, Molina J S, Pereperez J A

出版信息

Arch Intern Med. 1981 Mar;141(4):509-10. doi: 10.1001/archinte.141.4.509.

Abstract

Two patients had IgA deficiency, giardiasis, and the HLA-B8 antigen. The family of patient 1 included members with juvenile-onset diabetes mellitus, adrenal insufficiency, pernicious anemia, and hypothyroidism, a combination of unusual diseases that has been reported previously to occur as a syndrome with IgA deficiency and the HLA-B8 antigen. This coincidence makes it likely that these two patients and the one family previously described have a common pathogenic base, the inheritance of an abnormal immune-response gene that is acquired with the HLA-B8 antigen as a result of genetic dysequilibrium.

摘要

两名患者患有IgA缺乏症、贾第虫病和HLA - B8抗原。患者1的家族成员中有青少年型糖尿病、肾上腺功能不全、恶性贫血和甲状腺功能减退患者,这种不寻常的疾病组合此前曾被报道作为一种与IgA缺乏症和HLA - B8抗原相关的综合征出现。这种巧合表明,这两名患者以及之前描述的那个家族可能有共同的致病基础,即由于基因不平衡而与HLA - B8抗原一起获得的异常免疫反应基因的遗传。

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