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[银屑病的遗传。2035份家族史分析]

[Inheritance of psoriasis. Analysis of 2035 family histories].

作者信息

Andressen C, Henseler T

出版信息

Hautarzt. 1982 Apr;33(4):214-7.

PMID:7096085
Abstract

Detailed pedigrees were established in 2,035 families with psoriasis, including 30 twin pairs, and evaluated by means of computer analysis. The following results on the devolution of psoriasis were drawn: the hypotheses of the irregular dominant and the bifactorial recessive inheritance appear to be inacceptable. The findings suggest a multifactorial etiology of psoriasis with a polygenic mode of inheritance. The risk for relatives to be affected by psoriasis is calculated.

摘要

为2035个银屑病家庭建立了详细的谱系,其中包括30对双胞胎,并通过计算机分析进行评估。得出了以下关于银屑病遗传的结果:不规则显性遗传和双因子隐性遗传的假设似乎不可接受。研究结果表明银屑病具有多因素病因,遗传方式为多基因遗传。计算了亲属患银屑病的风险。

相似文献

1
[Inheritance of psoriasis. Analysis of 2035 family histories].[银屑病的遗传。2035份家族史分析]
Hautarzt. 1982 Apr;33(4):214-7.
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Psoriasis in Norwegian twins: contribution of genetic and environmental effects.挪威双胞胎中的银屑病:遗传和环境因素的作用
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Evidence that a locus for familial psoriasis maps to chromosome 4q.家族性银屑病的一个基因座定位于4号染色体长臂的证据。
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Feasibility of establishing deletion of the late cornified envelope genes LCE3B and LCE3C as a susceptibility factor for psoriasis.将晚期角质化包膜基因LCE3B和LCE3C的缺失确定为银屑病易感性因素的可行性。
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Clin Rev Allergy Immunol. 2013 Apr;44(2):166-72. doi: 10.1007/s12016-012-8305-3.
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Deletion of LCE3C and LCE3B genes at PSORS4 does not contribute to susceptibility to psoriatic arthritis in German patients.PSORS4 上 LCE3C 和 LCE3B 基因缺失与德国银屑病关节炎患者的易感性无关。
Ann Rheum Dis. 2010 May;69(5):876-8. doi: 10.1136/ard.2009.108951. Epub 2009 May 12.