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一种先天性视网膜营养不良和扫视麻痹综合征——莱伯氏黑蒙的一个亚型。

A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.

作者信息

Moore A T, Taylor D S

出版信息

Br J Ophthalmol. 1984 Jun;68(6):421-31. doi: 10.1136/bjo.68.6.421.

Abstract

Three children who presented in infancy with a severe visual defect and absent or barely recordable electroretinograms, with relatively well preserved visually evoked cortical potentials, were subsequently found to have vertical and horizontal saccade palsies with head thrusts but relatively good visual acuity. These children, who were clearly different from other infants with congenital retinal dystrophy, were also developmentally delayed and had systemic motor and speech defects, but their visual prognosis was relatively good. The recognition of their saccade palsy was delayed because their poor visual attention in infancy was ascribed purely to the tapetoretinal degeneration. We consider these patients represent a clear subset of those patients who are diagnosed as having congenital retinal dystrophy or Leber's amaurosis.

摘要

三名婴儿期出现严重视力缺陷、视网膜电图缺失或几乎无法记录,但视觉诱发皮层电位相对保存良好的儿童,随后被发现存在垂直和水平扫视麻痹伴头部前冲,但视力相对较好。这些儿童明显不同于其他先天性视网膜营养不良的婴儿,他们也有发育迟缓以及全身性运动和言语缺陷,但其视觉预后相对较好。由于他们婴儿期较差的视觉注意力被单纯归因于视网膜色素变性,其扫视麻痹的诊断被延迟。我们认为这些患者代表了那些被诊断为先天性视网膜营养不良或莱伯氏黑蒙症患者中的一个明确亚组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ac/1040367/5f61255bce9a/brjopthal00150-0072-a.jpg

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