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先天性胼胝体发育不全患者的解剖和电生理表现。

Anatomical and electrophysiological manifestations in a patient with congenital corpus callosum agenesis.

机构信息

Neuroscience Laboratory, Department of Neurology, China Medical University Hospital, Taichung, Taiwan.

出版信息

Brain Topogr. 2013 Jan;26(1):171-6. doi: 10.1007/s10548-012-0247-9. Epub 2012 Aug 23.

Abstract

The corpus callosum is the major brain structure responsible for the transferring of information between the two hemispheres. In congenital agenesis of the corpus callosum (ACC), an alternative functional connection might exist between the hemispheres; however, this has yet to be demonstrated. The present study evaluated a 27-year-old man with ACC but no detectable motor function deficits using diffusion tensor imaging (DTI), movement-related cortical potential (MRCP), and interhemispheric inhibition (IHI). The MRCP was analyzed at the electrodes of C3, FCZ, and C4. IHI was measured using paired transcranial magnetic stimulation over the hand area of the primary motor cortex at both hemispheres. Data of the patient were compared with those of an age-matched healthy control group (n = 8, mean age: 27.6 ± 2.5 years). DTI showed absence of the callosal fibers and the presence of enhanced transcommissural fibers in the ACC patient. The mean fractional anisotropy of the transcommissural fibers revealed a significant difference between the patient and the control group (0.62 vs. 0.43, p < 0.01). The MRCP and IHI, supposed to be highly relevant to the transcallosal pathway, were present in the patient though they occurred to a relatively low degree compared to the control group. Findings suggest that in the ACC patient, the abnormal transcommissural fibers might be functional and serve as an alternative pathway connecting the bilateral hemispheres.

摘要

胼胝体是大脑中负责连接两个半球之间信息传递的主要结构。在胼胝体发育不全(ACC)中,两个半球之间可能存在替代的功能连接;然而,这一点尚未得到证实。本研究使用弥散张量成像(DTI)、运动相关皮质电位(MRCP)和半球间抑制(IHI)评估了一名 27 岁的 ACC 患者,但没有检测到运动功能缺陷。MRCP 在 C3、FCZ 和 C4 电极上进行分析。使用双侧初级运动皮质手部区域的经颅磁刺激对 IHI 进行测量。将患者的数据与年龄匹配的健康对照组(n=8,平均年龄:27.6±2.5 岁)进行比较。DTI 显示该 ACC 患者的胼胝体纤维缺失和胼胝体间纤维增强。Transcommissural 纤维的平均各向异性分数在患者和对照组之间存在显著差异(0.62 对 0.43,p<0.01)。MRCP 和 IHI 与胼胝体通路高度相关,尽管与对照组相比程度相对较低,但在患者中仍存在。这些发现表明,在 ACC 患者中,异常的胼胝体间纤维可能具有功能性,并作为连接双侧半球的替代途径。

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