青年中文pigmentosa的意思
pigmentosa中文翻譯：
n.眼點；色點（植）
retinitis pigmentosa───[眼科]色素性視網膜炎
About 100, 000 have retinitis pigmentosa, a progressive, genetic disorder that usually manifests in childhood.───約有10萬人患有視網膜色素變性疾病，它是一種進行性的遺傳疾病，通常在兒童時期發病。
Retinitis pigmentosa is a disease that causes progressive loss of vision, as the photoreceptor cells degenerate, and eventually die.───視網膜炎色斑是一種可以引起視力喪失的疾病，也就是圖像受體細胞退化，最終喪失功能。
Two of them suffered from retinitis pigmentosa, while the third had a similar disease.───其中的兩個患有視網膜炎色斑疾病，第三個患有類似的疾病。
It is so far being used in people with retinitis pigmentosa, in which photoreceptor cells, which take in light, deteriorate.───目前人工視網膜被用于患有色素性視網膜炎的病人，他們的光感受器細胞退化了。
Retinitis pigmentosa is an inherited disorder that accounts for 11% of cases of blindness and has no medical treatment.───色素性視網膜炎是一種遺傳性疾病，11%的病例中病人會完全失明并且沒有治療方法。
Retinitis pigmentosa is one hereditary disease that cause blind eyes and have relatively high incidence of disease.───視網膜色素變性是一種遺傳性致盲性眼病，發病率較高，危害性較大。
could eventually revolutionize the lives of up to 200, 000 people worldwide who suffer from blindness as a result of retinitis pigmentosa.───（它），最終可能改變的生活世界200000人遭受失明由于患有色素性視網膜炎。
She says there was a study which suggested that vitamin A helped some people with retinitis pigmentosa.───但她還說道，以前曾有實驗證明維生素A可以幫助部分人群抵御色素性視網膜炎。
Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).───目的確定常染色體顯性遺傳視網膜色素變性家系的致病基因及其突變位點，并研究其臨床表型。
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.