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DOI 10.1007/s11682-016-9517-6

Медицинская библиотека · Brain imaging and behavior · 2017

Cortical damage in the posterior visual pathway in patients with sialidosis type 1.

Lu Chin-Song, Ng Shu-Hang, Lai Szu-Chia, Kao Ling-Yuh, Liu Laura, Lin Wey-Yil, Wu Yi-Ming, Chen Yao-Liang, Wang Jiun-Jie

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

In order to identify the cortical changes in patients with Sialidosis type 1, diffusion tensor imaging and resting state fMRI were acquired from 11 patients and 11 sex/age matched normal controls after clinical evaluations. The neuroimages from each participant were normalized and parcellated according to the Automatic Anatomical Labeling. Both the mean diffusivity and the corresponding functional connectivity were calculated from each cortical region. The white matter tract integrity was examined. The difference between patients and controls was examined using Student's t-test and between patients with either homozygous or heterozygous mutations by Mann-Whitney U test, both at a threshold of 0.05. Increased mean diffusivity throughout the brain can be noticed in the patients, together with a compromised white matter tracts integrity. The most severely affected cortical regions are in the occipital lobe. Decreased functional connectivity was from the temporal and occipital lobes to the hippocampus and parahippocampus. In contrast, connectivity from thalamus was enhanced. Diffused cortical atrophy with posterior focal lesions was noticed. We concluded that MRI observed functional changes in the posterior cortical pathways in the patients with Sialidosis. The observation might be related to the cortical blindness due to an altered neural network and a compromised visual pathway in the patients.

Для цитирования: Lu Chin-Song, Ng Shu-Hang, Lai Szu-Chia, Kao Ling-Yuh, Liu Laura, Lin Wey-Yil, Wu Yi-Ming, Chen Yao-Liang, Wang Jiun-Jie. Cortical damage in the posterior visual pathway in patients with sialidosis type 1.. Brain imaging and behavior. 2017. DOI: 10.1007/s11682-016-9517-6.

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