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[显性遗传性青少年视神经萎缩的视觉功能]

[Visual functions of dominantly inherited juvenile optic atrophy].

作者信息

Terasaki H, Miyake Y, Awaya S, Horio N

机构信息

Department of Ophthalmology, Nagoya University School of Medicine, Aichi-ken, Japan.

出版信息

Nippon Ganka Gakkai Zasshi. 1995 Aug;99(8):964-71.

PMID:7676899
Abstract

Visual functions including color vision and spectral sensitivity were investigated in 18 of 36 patients and in 2 persons with normal visual acuity in 8 families with dominantly inherited juvenile optic atrophy. Seven of the 8 families had at least one member who showed mainly acquired blue-yellow color vision deficiency. However, only 4 patients showed typical blue-yellow color vision deficiency, which suggested nonspecific characteristics of color vision deficiency in optic neural diseases. One family showed mainly acquired red-green color vision deficiency. Spectral sensitivity functions measured in 5 patients of 3 families showed sensitivity loss in the middle and long wavelength range as well as markedly decreased sensitivity in the short wavelength range. Decrease in spectral sensitivity in the short wavelength range or minimal blue-yellow color vision defect in a subject's brothers with normal visual acuity is interesting, but further study is needed because blue sensitivity decreases easily in various conditions.

摘要

在8个患有显性遗传性青少年视神经萎缩的家族中,对36例患者中的18例以及2例视力正常者进行了包括色觉和光谱敏感度在内的视觉功能研究。8个家族中有7个家族至少有一名成员主要表现为后天性蓝黄色觉缺陷。然而,只有4例患者表现出典型的蓝黄色觉缺陷,这表明视神经疾病中色觉缺陷具有非特异性特征。有一个家族主要表现为后天性红绿色觉缺陷。在3个家族的5例患者中测量的光谱敏感度函数显示,中长波长范围内敏感度降低,短波长范围内敏感度明显下降。视力正常的受试者兄弟在短波长范围内光谱敏感度降低或蓝黄色觉缺陷轻微,这很有意思,但由于在各种情况下蓝色敏感度很容易降低,因此需要进一步研究。

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