Rauscher Franziska G, Plant Gordon T, James-Galton Merle, Barbur John L
Applied Vision Research Centre, Henry Wellcome Laboratories for Vision Sciences City University, Northampton Square, London, United Kingdom.
Visual Disorders Group, The National Hospital for Neurology and Neurosurgery, Queen Square, London, United Kingdom.
Neuroophthalmology. 2011 Jan 16;35(1):1-6. doi: 10.3109/01658107.2010.540767. eCollection 2011.
Damage to ventral occipito-temporal extrastriate visual cortex leads to the syndrome of prosopagnosia often with coexisting cerebral achromatopsia. A patient with this syndrome resulting in a left upper homonymous quadrantanopia, prosopagnosia, and incomplete achromatopsia is described. Chromatic sensitivity was assessed at a number of locations in the intact visual field using a dynamic luminance contrast masking technique that isolates the use of colour signals. In normal subjects chromatic detection thresholds form an elliptical contour when plotted in the Commission Internationale d'Eclairage, (x-y), chromaticity diagram. Because the extraction of colour signals in early visual processing involves opponent mechanisms, subjects with Daltonism (congenital red/green loss of sensitivity) show symmetric increase in thresholds towards the long wavelength ("red") and middle wavelength ("green") regions of the spectrum locus. This is also the case with acquired loss of chromatic sensitivity as a result of retinal or optic nerve disease. Our patient's results were an exception to this rule. Whilst his chromatic sensitivity in the central region of the visual field was reduced symmetrically for both "red/green" and "yellow/blue" directions in colour space, the subject's lower left quadrant showed a marked asymmetry in "red/green" thresholds with the greatest loss of sensitivity towards the "green" region of the spectrum locus. This spatially localized asymmetric loss of "green" but not "red" sensitivity has not been reported previously in human vision. Such loss is consistent with selective damage of neural substrates in the visual cortex that process colour information, but are spectrally non-opponent.
枕颞叶腹侧纹外视觉皮层受损会导致人面失认症综合征,常伴有并存的脑性全色盲。本文描述了一名患有该综合征的患者,其出现左上象限同侧偏盲、人面失认症和不完全性全色盲。使用一种动态亮度对比掩蔽技术在完整视野的多个位置评估了色觉敏感度,该技术可分离颜色信号的使用情况。在正常受试者中,当在国际照明委员会(CIE)的(x - y)色度图中绘制时,色觉检测阈值形成一个椭圆形轮廓。由于早期视觉处理中颜色信号的提取涉及拮抗机制,患有色盲症(先天性红/绿敏感度丧失)的受试者在光谱轨迹的长波长(“红色”)和中波长(“绿色”)区域的阈值对称增加。视网膜或视神经疾病导致的后天性色觉敏感度丧失也是如此。我们患者的结果是个例外。虽然他在视野中央区域对颜色空间中“红/绿”和“黄/蓝”方向的色觉敏感度均对称降低,但受试者的左下象限在“红/绿”阈值上表现出明显的不对称,对光谱轨迹的“绿色”区域敏感度损失最大。这种在空间上局部化的“绿色”而非“红色”敏感度的不对称丧失在人类视觉中此前尚未有报道。这种丧失与处理颜色信息但在光谱上非拮抗的视觉皮层神经基质的选择性损伤一致。