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假性剥脱性青光眼的遗传学、诊断与监测

Genetics, Diagnosis, and Monitoring of Pseudoexfoliation Glaucoma.

作者信息

Nathan Niraj, Kuchtey Rachel W

机构信息

2311 Pierce Ave, Nashville, TN 37232-8808, 615-936-2020, 615-936-1540 (Fax),

2311 Pierce Ave, Nashville, TN 37232-8808.

出版信息

Curr Ophthalmol Rep. 2016 Dec;4(4):206-212. doi: 10.1007/s40135-016-0113-0. Epub 2016 Oct 11.

Abstract

Recent studies have shed new light on the genetic factors underlying pseudoexfoliation syndrome, growing our understanding of the role of the lysyl oxidase-like 1 (LOXL1) gene and its various polymorphisms as well as identifying new genetic associations. Recent years have brought new insight on how these genetic factors interact with other factors, including environmental, to confer risk to individuals and populations worldwide. All of these findings may hold importance to the screening, diagnosis, and monitoring of pseudoexfoliation and may also help lead to the identification of novel therapeutic targets. This review serves as an update on the recent trends and findings in pseudoexfoliation syndrome.

摘要

最近的研究为假性剥脱综合征背后的遗传因素带来了新的认识,加深了我们对赖氨酰氧化酶样1(LOXL1)基因及其各种多态性作用的理解,并确定了新的遗传关联。近年来,对于这些遗传因素如何与包括环境因素在内的其他因素相互作用,从而使全球个体和人群面临风险,有了新的见解。所有这些发现可能对假性剥脱的筛查、诊断和监测具有重要意义,也可能有助于识别新的治疗靶点。本综述对假性剥脱综合征的最新趋势和发现进行了更新。

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Genetics, Diagnosis, and Monitoring of Pseudoexfoliation Glaucoma.假性剥脱性青光眼的遗传学、诊断与监测
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