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Mills Syndrome Clinical and Radiologic Asymmetry

机译:米尔斯综合症临床和放射不对称

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摘要

A 58-year-old man presented with a 3-year history of minimally progressive right-sided weakness. Examination revealed facial asymmetry, mild pyramidal weakness in the upper and lower limbs with spasticity, brisk reflexes, and upgoing plantar on the right only. Sensory examination was normal. MRI brain abnormalities are demonstrated (figures 1 and 2 and video). Serial EMG of the limbs and motor unit number estimation were symmetrically normal without evidence of concurrent lower motoneuron (LMN) pathology. Unilateral midbrain atrophy in Mills syndrome is rarely reported. The current case illustrates the associated asymmetric reduction in corticospinal tract fibers and absence of LMN involvement, further supporting a hemiparetic variant of primary lateral sclerosis.

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