Tager-Flusberg H, Boshart J, Baron-Cohen S
The Shriver Center, Department of Behavioral Sciences, Waltham, MA 02154, USA.
J Cogn Neurosci. 1998 Sep;10(5):631-9. doi: 10.1162/089892998563031.
This study tested the hypothesis that Williams syndrome, a rare genetic neurodevelopmental disorder with an unusual cognitive phenotype, involves spared abilities in the domain of understanding other minds. A group of retarded adults with Williams syndrome was compared to an age-, IQ-, and language-matched group of adults with Prader-Willi syndrome, another genetic disorder without the cognitive characteristics of Williams syndrome, and a group of age-matched normal adults, on a task that taps mentalizing ability. The task involved selecting the correct labels to match photographs of complex mental state expressions in the eye region of the face. The adults with Williams syndrome performed significantly better than the adults with Prader-Willi on this task, and about half the group performed in the same range as the normal adults. These findings are consistent with anecdotal evidence about Williams syndrome and provide evidence that mentalizing is a distinct cognitive domain. This spared cognitive capacity may be linked to the relative sparing of limbic-cerebellar neural substrate in Williams syndrome, which is also connected to cortico-frontal regions that are known to be involved in understanding complex mental states.
威廉姆斯综合征,一种罕见的具有特殊认知表型的遗传性神经发育障碍,在理解他人心理领域存在保留能力。将一组患有威廉姆斯综合征的智障成年人与一组年龄、智商和语言相匹配的普拉德-威利综合征成年人(另一种没有威廉姆斯综合征认知特征的遗传性疾病)以及一组年龄匹配的正常成年人进行比较,完成一项测试心理理论能力的任务。该任务要求选择正确的标签来匹配面部眼部区域复杂心理状态表情的照片。患有威廉姆斯综合征的成年人在这项任务中的表现明显优于患有普拉德-威利综合征的成年人,并且该组中约一半人的表现与正常成年人处于同一水平。这些发现与关于威廉姆斯综合征的轶事证据一致,并提供了心理理论是一个独特认知领域的证据。这种保留的认知能力可能与威廉姆斯综合征中边缘小脑神经基质的相对保留有关,而边缘小脑神经基质也与已知参与理解复杂心理状态的皮质额叶区域相连。