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先天性静止性夜盲症中的视网膜电图振荡电位丧失、视神经萎缩和发育异常。

Loss of electroretinographic oscillatory potentials, optic atrophy, and dysplasia in congenital stationary night blindness.

作者信息

Heckenlively J R, Martin D A, Rosenbaum A L

出版信息

Am J Ophthalmol. 1983 Oct;96(4):526-34. doi: 10.1016/s0002-9394(14)77917-6.

Abstract

New criteria for diagnosing congenital stationary night blindness include loss of the oscillatory potentials in the photopic and bright-flash dark-adapted electroretinogram, and atrophy or dysplastic changes, or both, in the optic nerve head. Ten patients (seven male and three female, ranging in age from 6 to 19 years) had typical findings of congenital stationary night blindness including congenital nonprogressive nyctalopia, no pigmentary retinopathy, and full visual fields consistent with myopia. Visual acuities ranged from 20/30 to 20/60, though one patient had a visual acuity of 20/200. Most patients had histories of strabismus. The photopic electroretinograms were subnormal. Of the male patients, five had tilted optic disks with temporal portions of the nerve missing, and two had misshapen nerve heads. The three female patients had pallor of the optic disk without evidence of tilt.

摘要

先天性静止性夜盲的诊断新标准包括

明视和闪光暗适应视网膜电图中振荡电位消失,以及视神经乳头萎缩或发育异常改变,或两者皆有。10例患者(7例男性,3例女性,年龄6至19岁)有先天性静止性夜盲的典型表现,包括先天性非进行性夜盲、无色素性视网膜病变以及与近视相符的完整视野。视力范围为20/30至20/60,不过有1例患者视力为20/200。大多数患者有斜视病史。明视视网膜电图异常。男性患者中,5例视盘倾斜,神经颞侧部分缺失,2例神经乳头形状异常。3例女性患者视盘苍白,无倾斜迹象。

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