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- W4386822823 abstract "Case presentation: A previously healthy boy, aged 3 years and 2 months, with no relevant perinatal or personal history and with normal neuropsychomotor development, started with monoparesis of the right lower limb that evolved in 4 days to hemiparesis without change in level of consciousness or behavior. Neurological examination showing hemiparetic gait. Hyperreflexia, more evident in right hemibody members. Absence of Babinski sign. Screening laboratory tests were normal. Brain MRI showed diffuse hyperintensity on T2/FLAIR white matter, extending through the temporal, occipital and bilateral parietal regions, more markedly on the left, with bilateral punctate areas of contrast medium uptake. In view of the initial condition, corticosteroid therapy was initiated with complete remission of hemiparesis in 3 days. It was then decided to maintain corticosteroid therapy and complement the investigation with an anti-MOG antibody test whose result was positive. He maintained a normal neurological exam in the outpatient visits and control MRI showed improvement in the lesions." @default.
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- W4386822823 date "2023-09-01" @default.
- W4386822823 modified "2023-09-26" @default.
- W4386822823 title "An atypical phenotype of myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD)" @default.
- W4386822823 doi "https://doi.org/10.1055/s-0043-1774611" @default.
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