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首页> 外文期刊>Contact dermatitis >The genetics of allergic contact hypersensitivity to nickel.
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The genetics of allergic contact hypersensitivity to nickel.

机译:对镍过敏接触的遗传学。

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摘要

We have examined evidence for familial disposition to nickel allergic contact dermatitis (Ni ACD). 258 patients attending for routine patch testing were recruited prospectively. 39 patients were diagnosed with Ni ACD. 31 of 209 1st-degree relatives (15%) of probands had a history of nickel hypersensitivity. 84 patients with no history of nickel hypersensitivity and negative patch tests to nickel were used as controls. 24 of 458 1st degree relatives of controls (5.2%) had a history of Ni ACD. The risk ratio for 1st degree relatives of a patient with Ni ACD is 2.83 (95% confidence intervals are 2.45, 3.27). This is the 1st study to present a statistic to represent risk to relatives of developing ACD. Relatives of patients with Ni ACD have an increased risk of developing the condition, but the genetic basis for this is not yet known. With currently available techniques, this value of relative risk makes a positional cloning approach to gene identification impractical.
机译:我们检查了家族成员对镍过敏性接触性皮炎(Ni ACD)的治疗倾向。前瞻性招募了258名参加常规斑贴试验的患者。 39例患者被诊断患有Ni ACD。 209名一级亲戚中有31名(15%)有镍过敏史。 84例无镍过敏史且对镍的斑贴试验阴性。 458名一级直系亲属中有24名(5.2%)有Ni ACD病史。 Ni ACD患者一级亲属的风险比是2.83(95%置信区间是2.45,3.27)。这是第一个提出统计数据来代表发展为ACD的亲属的风险的研究。 Ni ACD患者的亲戚患病的风险增加,但是其遗传基础尚不清楚。利用当前可用的技术,这种相对风险的值使得基因克隆的位置克隆方法不可行。

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