首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Does dominance of crossing retinal ganglion cells make the eyes cross? The temporal retina in the origin of infantile esotropia – a neuroanatomical and evolutionary analysis
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Does dominance of crossing retinal ganglion cells make the eyes cross? The temporal retina in the origin of infantile esotropia – a neuroanatomical and evolutionary analysis

机译:视网膜神经节细胞交叉的优势是否会使眼睛交叉?婴幼儿内斜视起源的颞视网膜-神经解剖学和进化分析

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摘要

A closer look at the evolution of the eye and the brain provides a possible explanation for both the origin of infantile esotropia and its motor characteristics. In the course of evolution, the eyes have moved from a lateral to a frontal position. Consequently, the monocular visual fields started to overlap resulting in a binocular visual field. In lateral-eyed animals, the retinae project to the contralateral visual cortices only. These projections are also found in binocular mammals and birds with binocular visual fields but in addition there are uncrossed projections from the temporal retinae to the visual cortex. The partial chiasmal decussation and the corpus callosum provide the necessary structure that allows binocular vision to develop. Disruption of normal binocular development causes a loss of binocularity in the primary visual cortex and beyond. Beyond the primary visual cortex, the contralateral eye dominates while the temporal retinal signal appears to lose influence. Loss or absence of binocular vision in infantile esotropia may be caused by inadequate retinotopic matching between the nasal and temporal retinal signals like in albinism with an abnormal or asymmetric chiasmal decussation or agenesis of the corpus callosum. Dominance of the crossing retinal signal might also explain the motor characteristics of infantile esotropia (asymmetric OKN, latent nystagmus, DVD). A normal binocular cortical signal will predominate over the evolutionary older, originally non-binocular, retinal projections to the superior colliculi (CS) and the accessory optic system (AOS). A suppressed temporal retinal signal paves the way for the re-emergence of eye movements driven by one eye, as in lateral-eyed non-binocular animals.
机译:仔细观察眼睛和大脑的演变,可以为婴儿内斜视的起源及其运动特征提供可能的解释。在进化过程中,眼睛从侧面位置移到了正面位置。因此,单眼视野开始重叠,形成双眼视野。在侧眼动物中,视网膜仅投射到对侧视皮层。在具有双眼视野的双目哺乳动物和鸟类中也发现了这些投影,但是此外,从颞视网膜到视觉皮层还有不交叉的投影。局部裂痕和cus体提供了必要的结构,使双眼视觉得以发展。正常的双眼发育中断会导致初级视觉皮层及以后的双眼丧失。除初级视觉皮层外,对侧眼占优势,而颞视网膜信号似乎失去影响。婴儿内斜视中双眼视力的丧失或缺失可能是由于鼻和时域视网膜信号之间的视网膜原位匹配不足所致,例如白化病伴有异常或不对称的as骨排列或cus体发育不全。视网膜交叉信号的优势也可能解释了婴儿内斜视的运动特征(不对称OKN,潜在性眼球震颤,DVD)。正常的双眼皮层信号将优先于上丘骨(CS)和辅助视神经系统(AOS)的演化的较老的,最初是非双眼的视网膜投影。如在侧眼非双眼动物中一样,抑制的暂时性视网膜信号为由一只眼睛驱动的眼球运动的重新出现铺平了道路。

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