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- W4214733239 abstract "We present an adult case of mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). A 26-year-old man with a family history of MERS presented to our hospital owing to dysarthria and dysesthesia of the right side of his body. The duration of these symptoms was approximately 4 hours. T2 and diffusion weighted MRI showed high signal intensity lesions in the bilateral deep white matter. On a 3-week follow-up MRI, the lesions had completely disappeared. We attributed this clinical course and image findings to MERS. The patient had experienced similar symptoms at the age of 8 years old. Furthermore, his younger brother showed a similar clinical history and experienced a few recurrence events during the age of 9-16 years old. The mechanism of MERS remains controversial. However, similar to our case, there are some case reports with a family history. In addition, a previous report has confirmed the existence of a heterozygous variant in the myelin regulatory factor gene in patients with MERS. Some genetic factors may induce MERS, especially with extensive white matter lesions." @default.
- W4214733239 created "2022-03-02" @default.
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- W4214733239 date "2021-01-01" @default.
- W4214733239 modified "2023-10-16" @default.
- W4214733239 title "Mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) with a family history: an adult case" @default.
- W4214733239 doi "https://doi.org/10.5692/clinicalneurol.cn-001697" @default.
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