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不稳定的前突变可能解释了色素失禁症在男性中的嵌合疾病表现。

Unstable pre-mutation may explain mosaic disease expression of incontinentia pigmenti in males.

作者信息

Traupe H, Vehring K H

机构信息

Department of Dermatology, University of Münster, Germany.

出版信息

Am J Med Genet. 1994 Feb 15;49(4):397-8. doi: 10.1002/ajmg.1320490409.

Abstract

Mosaic skin lesions following the lines of Blaschko are found in boys affected by incontinentia pigmenti (IP). For an X-linked gene defect, this is rather surprising. To explain the mosaic disease expression of IP in males, we propose that the disease is caused by an unstable pre-mutation, which normally remains silent in males during early embryogenesis. Occasionally "silencing" is incomplete and gives rise to clinical manifest IP reflecting a mosaic state of alleles with the full and the pre-mutation in the same patient. This model can account for mother-to-son transmission of IP and for disparate phenotypes in monozygotic female twins.

摘要

患有色素失禁症(IP)的男孩身上发现了沿Blaschko线分布的镶嵌性皮肤病变。对于一种X连锁基因缺陷来说,这相当令人惊讶。为了解释IP在男性中的镶嵌性疾病表现,我们提出该疾病是由一种不稳定的前突变引起的,这种前突变在男性早期胚胎发育过程中通常保持沉默。偶尔,“沉默”并不完全,会导致临床显性的IP,反映出同一患者中具有完全突变和前突变的等位基因的镶嵌状态。该模型可以解释IP的母传子现象以及同卵双胞胎女性中不同的表型。

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