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- Keywords multifocal electroretinogram;first kernel response;primary retinitis pigmentosa; 多焦视网膜电图;一阶反应;原发性视网膜色素变性;
- primary retinitis pigmentosa 原发性色素性视网膜炎
- Ik denk het wordt geroepen retinitis pigmentosa. 我闻悉它某处。我接受提名为adminship 。
- 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。
- Patients with retinitis pigmentosa typically experience nyctalopia in adolescence or early adulthood because of primary degeneration of their rods. 其主要临床特征为夜盲、进行性视野缺损、眼底色素沉着和视网膜电图异常或无波等。
- 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。
- 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。
- Objective: To study the effects of rhodopsin (RHO) gene in autosomal dominant retinitis pigmentosa (adRP). 摘要目的：探讨视紫红质基因在视网膜色素变性疾病中的作用。
- Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence of 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。
- It changed the codon CGA for Arginine to a terminator codon TGA and causes retinitis pigmentosa in the two families. 它使该基因编码精氨酸的遗传密码CGA变为终止密码TGA,引起发病。
- 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。
- 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。
- 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 ( 5 5 67%25 )。 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。
- Objective To identify the disease locus in X-linked retinitis pigmentosa (RP) families using genetic linkage analysis. 目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析,定位其致病基因的所在位点。
- X-linked retinitis pigmentosa is the most devastating form of RP because of its severe clinical manifestations. 染色体连锁遗传RP作为其中的一种类型,具有发病早,损害最为严重等特点。
- Retinitis pigmentosa (RP) is a common genetic eye disease affecting about 1 in 3500 people the worldwide. 视网膜色素变性是一组常见的遗传性致盲眼病,患病率约为1／3500。
- Objective To identify the disease locus in X-linked retinitis pigmentosa(XLRP) families using genetic linkage analysis. 目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析,确定其致病基因的所在位点。
- Retinitis pigmentosa (RP) is a common genetic eye disease affecting about 1 in 3500 people worldwide with pan-ethnic occurrence. 视网膜色素变性(rp)是遗传性致盲眼病,其患病率约为1/3500。
- The rare congenital condition of retinitis pigmentosa give rise to diffuse peripheral pigmentation with intervening pallor producing night, and later total, blindness. 少见的先天性色素性视网膜病变引起周边部位呈弥漫性色素沉着并杂以灰白色沉着于其间，而产生夜盲，到晚期导致全盲，即失明。
- Objective To investigate the characteristics of the multifocal electroretinogram (ERG) and to evaluate the application values of the multifocal ERG in retinitis pigmentosa (RP). 目的研究视网膜色素变性（RP）的多焦视网膜电图（ERG）特性和评价多焦ERG应用价值。
