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家族性亚历山大病中是否存在遗传预期?

Does genetic anticipation occur in familial Alexander disease?

机构信息

Department of Basic and Clinical Neuroscience, King's College London, London, UK.

Department of Neuroradiology, King's College Hospital NHS Trust, London, UK.

出版信息

Neurogenetics. 2021 Jul;22(3):215-219. doi: 10.1007/s10048-021-00642-9. Epub 2021 May 28.

Abstract

Alexander Disease (AxD) is a rare leukodystrophy caused by missense mutations of glial fibrillary acidic protein (GFAP). Primarily seen in infants and juveniles, it can present in adulthood. We report a family with inherited AxD in which the mother presented with symptoms many years after her daughter. We reviewed the age of onset in all published cases of familial AxD and found that 32 of 34 instances of parent-offspring pairs demonstrated an earlier age of onset in offspring compared to the parent. We suggest that genetic anticipation occurs in familial AxD and speculate that genetic mosaicism could explain this phenomenon.

摘要

亚历山大病(AxD)是一种罕见的脑白质营养不良,由神经胶质纤维酸性蛋白(GFAP)的错义突变引起。主要见于婴儿和青少年,但也可发生于成年期。我们报告了一个家族性 AxD 病例,其中母亲在女儿患病多年后出现症状。我们回顾了所有已发表的家族性 AxD 病例的发病年龄,发现 34 对父母-子女中,有 32 对子女的发病年龄早于父母。我们认为家族性 AxD 存在遗传早现现象,并推测遗传嵌合现象可能解释这一现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18cf/8241638/f0534a5f4cf3/10048_2021_642_Fig1_HTML.jpg

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