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威廉姆斯综合征和唐氏综合征患者磁共振图像上的异常脑形态。

Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.

作者信息

Jernigan T L, Bellugi U

机构信息

San Diego (Calif) Veterans Administration Medical Center, La Jolla.

出版信息

Arch Neurol. 1990 May;47(5):529-33. doi: 10.1001/archneur.1990.00530050049011.

Abstract

Quantitative studies of brain morphology in a group of subjects with Williams syndrome revealed a distinctive pattern of dysmorphology unlike that observed in another form of mental retardation. Down syndrome. Reduced cerebral size but normal cerebellar size was observed in Williams syndrome, in contrast to reductions in both brain components in Down syndrome. Examination of cerebellar vermal morphology suggested significantly increased area of neocerebellar vermal lobules in Williams syndrome, with low-normal size in the paleocerebellar vermal lobules. Thus, a highly selective effect on brain development appears to accompany Williams syndrome, with some brain subsystems, possibly later-developing ones, relatively spared.

摘要

对一组威廉姆斯综合征患者的大脑形态进行的定量研究显示,其畸形模式与众不同,与另一种智力迟钝——唐氏综合征中观察到的情况不同。在威廉姆斯综合征中观察到大脑尺寸减小但小脑尺寸正常,而唐氏综合征中大脑的两个组成部分均减小。对小脑蚓部形态的检查表明,威廉姆斯综合征中新小脑蚓部小叶的面积显著增加,而旧小脑蚓部小叶的尺寸略低于正常水平。因此,威廉姆斯综合征似乎伴随着对大脑发育的高度选择性影响,一些大脑子系统,可能是较晚发育的子系统,相对未受影响。

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