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前极性白内障:一个家族中的临床谱及基因连锁关系

Anterior polar cataract: clinical spectrum and genetic linkage in a single family.

作者信息

Ionides A, Berry V, Mackay D, Shiels A, Bhattacharya S, Moore A

机构信息

Department of Molecular Genetics Institute of Ophthalmology London, UK.

出版信息

Eye (Lond). 1998;12 ( Pt 2):224-6. doi: 10.1038/eye.1998.53.

Abstract

Anterior polar cataract can occur as a sporadic finding, in association with other ocular abnormalities or as an inherited, autosomal dominant disorder. We have demonstrated linkage in a family with autosomal dominant anterior polar cataract to the short arm of chromosome 17, locating the gene to the region 17p12-13. All affected members of this large family had an opacity at the anterior pole of the lens that varied only in size and the effect on visual acuity. Anterior polar cataract is thought to have a minimal effect on visual acuity although in the affected members of this family there was a high incidence of unilateral amblyopia.

摘要

前极性白内障可作为散发性发现出现,与其他眼部异常相关,或作为一种遗传性常染色体显性疾病出现。我们已经在一个患有常染色体显性前极性白内障的家族中证实了与17号染色体短臂的连锁关系,将该基因定位到17p12 - 13区域。这个大家庭的所有受影响成员在晶状体前极都有混浊,仅在大小和对视力的影响方面有所不同。前极性白内障被认为对视力影响极小,尽管在这个家族的受影响成员中,单眼弱视的发生率很高。

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