| X-连锁遗传视网膜色素变性相关基因研究概况 |
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| 引用本文： | 李春霞,盛迅伦.X-连锁遗传视网膜色素变性相关基因研究概况[J].眼科新进展,2008,28(11):867-871. |
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| 作者姓名： | 李春霞 盛迅伦 |
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| 作者单位： | 1. 宁夏医学院附属医院眼科,宁夏回族自治区银川市,750004
2. 山东省青岛市经济技术开发区第一人民医院眼科,266555 |
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| 摘 要： | 视网膜色素变性(retinitis pigmentosa,RP)是视网膜光感受器细胞和色素上皮细胞变性导致夜盲和进行性视野缺损的一组具有临床亚型的基因遗传性致盲眼底病。至今,X-连锁RP已定位6个致病基因,并克隆了2个基因(RP2和RP3)。本文对X连锁型RP的遗传基因研究进展予以综述。
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| 关 键 词： | X-连锁 视网膜色素变性 基因位点 |
Related genes study on X-linked retinitis pigmentosa |
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| LI Chun-Xia,SHENG Xun-Lun.Related genes study on X-linked retinitis pigmentosa[J].Recent Advances in Ophthalmology,2008,28(11):867-871. |
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| Authors: | LI Chun-Xia SHENG Xun-Lun |
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| Abstract: | Retinitis pigmentosa(RP) is a group of genetically clinical hypotype eyeground disorders that are characterized with night blind and progressed visual field defect by degeneration of retinal photoreceptor cell and pigment epithelium.Six virulence genes associated with X-linked RP have been located,and two genes(RP2 and RP3) have been cloned.This article reviews advances of research on X-linked RP genes. |
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| Keywords: | X-linked retinitis pigmentosa genetic spots |
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