先天性视锥细胞功能障碍。
Congenital cone dysfunction.
作者信息
Bartlett J D
出版信息
Am J Optom Physiol Opt. 1979 Mar;56(3):206-10. doi: 10.1097/00006324-197903000-00011.
Abstract
Three patients with congenital cone dysfunction are described with their clinical findings, including electrophysiologic and color vision evaluation, diagnostic criteria, and rehabilitative regimes. A classification system for this rare spectrum of disorders is presented.
摘要
本文描述了三名先天性视锥细胞功能障碍患者的临床检查结果，包括电生理和色觉评估、诊断标准及康复方案。并提出了针对这一罕见疾病谱的分类系统。
相似文献
1
Congenital cone dysfunction.先天性视锥细胞功能障碍。
Am J Optom Physiol Opt. 1979 Mar;56(3):206-10. doi: 10.1097/00006324-197903000-00011.
2
[A case of rod monochromasia].
Vestn Oftalmol. 2011 Nov-Dec;127(6):46-7.
3
Differential diagnosis of typical and atypical congenital achromatopsia. Analysis of a progressive foveal dystrophy and a nonprogressive oligo-cone trichromasy (general cone dysfunction without achromatopsia), both of which at first had been diagnosed as achromatopsia.典型与非典型先天性全色盲的鉴别诊断。对一种进行性黄斑营养不良和一种非进行性少视锥三色视觉（无全色盲的一般性视锥功能障碍）的分析，这两种情况最初都被诊断为全色盲。
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1978 Dec 8;209(1):19-28. doi: 10.1007/BF00419159.
4
Differential diagnosis of congenital tritanopia and dominantly inherited juvenile optic atrophy.先天性蓝色盲与显性遗传性青少年视神经萎缩的鉴别诊断。
Arch Ophthalmol. 1985 Oct;103(10):1496-501. doi: 10.1001/archopht.1985.01050100072022.
5
[Molecular genetic findings in patients with congenital cone dysfunction. Mutations in the CNGA3, CNGB3, or GNAT2 genes].[先天性视锥细胞功能障碍患者的分子遗传学发现。CNGA3、CNGB3或GNAT2基因突变]
Ophthalmologe. 2004 Aug;101(8):830-5. doi: 10.1007/s00347-003-0976-y.
6
[Study on classification and assessment of the degree of congenital color deficiencies using the 40 Hue Test devised as a color aptitude test and minute test].
Nippon Ganka Gakkai Zasshi. 1986 Jul;90(7):948-60.
7
8
[Clinical value of the differential diagnosis between congenital and acquired color blindness].
Bull Soc Ophtalmol Fr. 1980 Aug-Sep;80(8-9):679-81.
9
[Diagnostic difficulties in congenital achromatopsia].
Klin Oczna. 1982 Apr;84(4):109-10.
10
Application of the spatiochromatic visual evoked potential to detection of congenital and acquired color-vision deficiencies.
J Opt Soc Am A Opt Image Sci Vis. 1993 Aug;10(8):1818-25. doi: 10.1364/josaa.10.001818.
Zotero 插件