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家族性和散发性肌萎缩侧索硬化症的遗传学研究进展。

Recent advances in the genetics of familial and sporadic ALS.

机构信息

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

Department of Neurology, Columbia University, New York, NY, United States.

出版信息

Int Rev Neurobiol. 2024;176:49-74. doi: 10.1016/bs.irn.2024.04.007. Epub 2024 May 22.

Abstract

ALS shows complex genetic inheritance patterns. In about 5% to 10% of cases, there is a family history of ALS or a related condition such as frontotemporal dementia in a first or second degree relative, and for about 80% of such people a pathogenic gene variant can be identified. Such variants are also seen in people with no family history because of factor influencing the expression of genes, such as age. Genetic susceptibility factors also contribute to risk, and the heritability of ALS is between 40% and 60%. The genetic variants influencing ALS risk include single base changes, repeat expansions, copy number variants, and others. Here we review what is known of the genetic landscape and architecture of ALS.

摘要

肌萎缩侧索硬化症(ALS)表现出复杂的遗传继承模式。约 5%至 10%的病例存在 ALS 家族史或一级或二级亲属中存在额颞叶痴呆等相关疾病,大约 80%的此类人群可识别出致病性基因突变。由于影响基因表达的因素(如年龄),这些变异也存在于没有家族史的人群中。遗传易感性因素也会增加患病风险,ALS 的遗传率在 40%至 60%之间。影响 ALS 风险的遗传变异包括单碱基变化、重复扩展、拷贝数变异等。在这里,我们回顾了已知的 ALS 遗传景观和遗传结构。

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