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- enythrosis pigmentosa faciei 色素性面红斑
- 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。
- Urticaria pigmentosa with neutrophil infiltration was diagnosed. 诊断为伴中性粒细胞浸润的色素性荨麻疹。
- 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。
- Results The detection of CD20,CD45RA and LZM in LMF were higher than that of normal tissues of faciei. 结果CD20,CD45RA和溶菌酶在颜面粟粒性狼疮中的表达明显高于正常对照组。
- 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 explore related factors and clinical characteristics of tinea faciei, as well as reduce misdiagnosis and mistreatment. 目的:探讨面癣发病的相关因素、临床特点及诊断,降低误诊率。方法:分析患者的一般资料、病史及临床表现。
- 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。
- Objective To observe the effect of pigmentosa retinae treated by Chinese herb medicine point injection. 目的观察中药配合穴位注射治疗视网膜色素变性的临床疗效。
- 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。
- The mouse bid handles , finds out a pigmentosa about of each the central Shaanxi plain and color. 虽然又简单又无聊，你想过关，还真不容易。
- Methods 60 patients with pigmentosa retinae(spleen and kidney deficiency)were randomly divided into two groups. 方法将60例脾肾阳虚型视网膜色素变性患者随机分为2组。
- 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。
