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特纳综合征顶叶亚区域的容积研究。

A volumetric study of parietal lobe subregions in Turner syndrome.

作者信息

Brown Wendy E, Kesler Shelli R, Eliez Stephan, Warsofsky Ilana S, Haberecht Michael, Reiss Allan L

机构信息

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Dev Med Child Neurol. 2004 Sep;46(9):607-9. doi: 10.1017/s0012162204001021.

Abstract

Turner syndrome, a genetic disorder that results from the complete or partial absence of an X chromosome in females, has been associated with specific impairment in visuospatial cognition. Previous studies have demonstrated a relationship between parietal lobe abnormalities and visuospatial deficits in Turner syndrome. We used high-resolution magnetic resonance imaging to measure parietal lobe subdivisions in 14 participants with Turner syndrome (mean age 13 years 5 months, SD 5 years) and 14 age-matched controls (mean age 13 years 5 months, SD 4 years 7 months) to localize neuroanatomical variations more closely. Scans were acquired and analyzed for 14 females with Turner syndrome. Analyses of variance were used to investigate differences in regional parietal lobes. Females with Turner syndrome showed a bilateral parietal lobe reduction, specifically in the superior parietal and postcentral gyri. Full-scale IQ scores were significantly positively correlated with postcentral tissue volume in the Turner syndrome group. Structural differences in the parietal lobe are localized specifically to the anterior and superior parietal lobe and might be related to the visuospatial and visuomotor deficits associated with Turner syndrome.

摘要

特纳综合征是一种由于女性X染色体完全或部分缺失而导致的遗传性疾病,与视觉空间认知的特定损害有关。先前的研究已经证明特纳综合征患者顶叶异常与视觉空间缺陷之间存在关联。我们使用高分辨率磁共振成像来测量14名特纳综合征患者(平均年龄13岁5个月,标准差5岁)和14名年龄匹配的对照组(平均年龄13岁5个月,标准差4岁7个月)的顶叶细分,以更精确地定位神经解剖学变异。对14名特纳综合征女性进行了扫描并分析。采用方差分析来研究顶叶区域的差异。特纳综合征女性表现出双侧顶叶缩小,特别是在顶上叶和中央后回。在特纳综合征组中,全量表智商得分与中央后回组织体积显著正相关。顶叶的结构差异具体定位于顶叶前部和上部,可能与特纳综合征相关的视觉空间和视觉运动缺陷有关。

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