Retinitis Pigmentosa

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.

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.

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.

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.

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

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

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.

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。

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。

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。

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.

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

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

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。

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