Retinitis Pigmentosa

Progress in the research of mutation of genetic intron and retinitis pigmentosa

基因内含子突变与视网膜色素变性的研究进展

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The retinitis pigmentosa ( RP ) is an hereditary disease which causes visual deficiency leading to blindness.

视网膜 色素 变性 是一种具有遗传性的致盲性眼病.

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RESULTS The parameter of EOG was lower in the patients with retinitis pigmentosa than in volunteers.

结果视网膜色素变性患者眼电图检测主要参数均低于对照组.

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Retinitis pigmentosa, or R. P, is a form of retinal degeneration.

视网膜炎或R. P是视网膜变性的一种.

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In the view of molecular genetics, there is considerable genetic heterogeneity in retinitis pigmentosa ( RP), suggesting that the same gene in different countries or ethnic groups, with differences in their pathogenicity.

在分子遗传学角度上，视网膜色素变性（RP）存在相当大的遗传异质性，提示同一个基因在不同的国家或种族中，其致病性具有差异性。

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The man from Brittany in France was diagnosed with retinitis pigmentosa 40 years ago.

通过利用藻类中首次发现的感光蛋白，一名完全失明男子的部分视力得到了恢复。40年前，这名来自法国布列塔尼的男子被诊断患有视网膜色素变性。

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CONCLUSION Detection of EOG may be available for evaluating condition of retinitis pigmentosa and bianzhengfenxing.

眼电图检测参数的主要特点是光峰电位下降(5567%).结论　眼电图检测可用于对视网膜色素变性患者病变程度评估和辨证分型.

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Construction of a single copy probe library of retinitis pigmentosa type 3 gene locus

遗传性视网膜色素变性3型基因位点单拷贝探针库的构建

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The trio , who had lost almost all of their vision due to retinitis pigmentosa ( RP ).

他们由于患有色素性视网膜炎 ( RP ) 而几乎丧失了所有的视力.

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Haplotype analysis of two families with X-linked retinitis pigmentosa

两例疑为X连锁型视网膜色素变性家系的单倍型分析研究

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Investigation on genetic linkage analysis of X-linked retinitis pigmentosa using microsatellite markers

应用微卫星多态位点对X连锁型视网膜色素变性疾病进行遗传连锁分析的研究

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Primary study of iontophoresis of zinc ion in treatment of retinitis pigmentosa

直流电锌离子导入治疗视网膜色素变性的初步报告

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For one patient, this was the first time he had seen anything in half a century, after his sight was destroyed by retinitis pigmentosa, a virus that attacks retinal cells.

其中一个盲人，自从他的视力被色素性视网膜炎（一种侵袭视网膜细胞的病毒引起的）所损坏后，这是他半个世纪以来，首次有了视觉。

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Objectives To evaluate the effects of tinted filter lens on the visual rehabilitation of blind and low vision patients induced by optic nerve atrophy, glaucoma and retinitis pigmentosa.

目的探讨滤光镜在视神经萎缩、青光眼和视网膜色素变性所致盲和低视力患者视觉康复中的作用。

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Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence disease.

视网膜色素变性是一种遗传性致盲性眼病,发病率较高,危害性较大.

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