Ullevålsalleen 4C, 0852 Oslo, Norway.
Brain Cogn. 2010 Mar;72(2):165-6; discussion 167-8. doi: 10.1016/j.bandc.2009.07.001. Epub 2009 Jul 30.
A recent study [Keri, S., & Benedek, G. (2009). Visual pathway deficit in female fragile x premutation carriers: A potential endophenotype. Brain and Cognition, 69, 291-295] has found Vernier acuity deficiencies together with contrast sensitivity defects consistent with a magnocellular deficit in female fragile x premutation carriers. This may appear to support the notion that Vernier acuity may serve as a test of magnocellular sensitivity. However, Vernier acuity deficiencies have been reported in other conditions (e.g., schizophrenia, amblyopia and cortical visual impairment) where there is little evidence for magnocellular deficits. The observation that Vernier acuity deficiencies can occur without magnocellular deficits indicates that Vernier acuity is not a reliable test of magnocellular sensitivity.
最近的一项研究[Keri, S., & Benedek, G. (2009). 女性脆弱 X 前突变携带者的视觉通路缺陷:一种潜在的内表型。大脑与认知, 69, 291-295]发现,女性脆弱 X 前突变携带者存在视差锐度缺陷和对比敏感度缺陷,这与大细胞缺陷一致。这似乎支持视差锐度可以作为大细胞敏感性测试的观点。然而,视差锐度缺陷也在其他情况下(例如精神分裂症、弱视和皮质视觉障碍)中被报道,而这些情况下几乎没有大细胞缺陷的证据。视差锐度缺陷可以在没有大细胞缺陷的情况下发生的观察结果表明,视差锐度不是大细胞敏感性的可靠测试。