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致力于鉴定区域性积聚性斜视中的基因。

Towards identification of genes in regionally accumulated strabismus.

作者信息

Preising Markus

机构信息

Department of Paediatric Ophthalmology, Strabismology and Ophthalmogenetics, University of Regensburg, Germany.

出版信息

Strabismus. 2002 Jun;10(2):157-61. doi: 10.1076/stra.10.2.157.8141.

Abstract

Strabismus, as an inherited disease, is a new challenge to the geneticist. Various forms of strabismus can be found in distantly related members of the same family, who usually report to local ophthalmologists and orthoptic centers very rarely. In addition, local ophthalmologists and orthoptic centers very rarely pay attention to the genetic aspects of strabismus. Therefore, the recruitment of suitable families to identify the underlying genes is the major drawback in this effort. Further problems arise from the mode of inheritance, which can formally be characterized as autosomal dominant with reduced penetrance in most families, but should be considered as multifactorial inheritance with a threshold combination of mutated alleles. The present paper deals with a method for using local accumulations of strabismus patients to circumvent the problems of small families and rare numbers of affected persons. The steps on the way to the identification of strabismus genes will be described.

摘要

斜视作为一种遗传性疾病,对遗传学家来说是一个新的挑战。在同一家族关系较远的成员中可发现各种形式的斜视,而这些成员通常很少向当地眼科医生和斜视矫正中心求诊。此外,当地眼科医生和斜视矫正中心也很少关注斜视的遗传方面。因此,招募合适的家族来确定潜在基因是这项工作的主要障碍。遗传模式引发了更多问题,在大多数家族中,其正式特征可被描述为常染色体显性遗传且外显率降低,但应被视为具有突变等位基因阈值组合的多因素遗传。本文探讨了一种利用斜视患者的局部聚集来规避小家系和患者数量稀少问题的方法。文中将描述鉴定斜视基因过程中的各个步骤。

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