pigmentosa信息详情
n.眼点；色点（植）
retinitis pigmentosa───[眼科]色素性视网膜炎
About 100, 000 have retinitis pigmentosa, a progressive, genetic disorder that usually manifests in childhood.───约有10万人患有视网膜色素变性疾病，它是一种进行性的遗传疾病，通常在儿童时期发病。
Retinitis pigmentosa is a disease that causes progressive loss of vision, as the photoreceptor cells degenerate, and eventually die.───视网膜炎色斑是一种可以引起视力丧失的疾病，也就是图像受体细胞退化，最终丧失功能。
Two of them suffered from retinitis pigmentosa, while the third had a similar disease.───其中的两个患有视网膜炎色斑疾病，第三个患有类似的疾病。
It is so far being used in people with retinitis pigmentosa, in which photoreceptor cells, which take in light, deteriorate.───目前人工视网膜被用于患有色素性视网膜炎的病人，他们的光感受器细胞退化了。
Retinitis pigmentosa is an inherited disorder that accounts for 11% of cases of blindness and has no medical treatment.───色素性视网膜炎是一种遗传性疾病，11%的病例中病人会完全失明并且没有治疗方法。
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。
could eventually revolutionize the lives of up to 200, 000 people worldwide who suffer from blindness as a result of retinitis pigmentosa.───（它），最终可能改变的生活世界200000人遭受失明由于患有色素性视网膜炎。
She says there was a study which suggested that vitamin A helped some people with retinitis pigmentosa.───但她还说道，以前曾有实验证明维生素A可以帮助部分人群抵御色素性视网膜炎。
Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).───目的确定常染色体显性遗传视网膜色素变性家系的致病基因及其突变位点，并研究其临床表型。
His vision was impaired in 1984 due to retinitis pigmentosa and he became legally blind in 1987.
Aside from his chronic eye condition retinitis pigmentosa, which significantly limits his peripheral and nighttime vision, Wynn is in good health.
Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence disease.
The retinitis pigmentosa ( RP ) is an hereditary disease which causes visual deficiency leading to blindness.
Retinitis pigmentosa, or R. P, is a form of retinal degeneration.
This paper presents the results of statistics and analysis of 580 eyes of patients with retinitis pigmentosa in which vision, visual field, dark adaptation and electroretinography (ERG) were examined.
Objective To identify the disease locus in X - linked retinitis pigmentosa ( XLRP ) families using genetic linkage analysis.
Objective To observe the effect of pigmentosa retinae treated by Chinese herb medicine point injection.
Laurence-Moon syndrome is a rare hereditary condition associated with retinitis pigmentosa, spastic paraplegia, hypogonadism and mental retardation.