Mild encephalopathy with reversible splenial lesions associated with a rotavirus infection
Monatsschrift fur Kinderheilkunde, ISSN: 1433-0474, Vol: 167, Issue: 7, Page: 626-630
2019
- 1Citations
- 8Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
We present the case of a 4 ½‑year-old boy with gastrointestinal symptoms and somnolence who was admitted to our hospital. The diagnostic magnetic resonance imaging (MRI) showed a restricted boomerang-shaped diffusion disorder in the splenium of the corpus callosum. The electroencephalograph (EEG) showed slow waves, fecal rotavirus antigen was positive, the cerebrospinal fluid (CSF) examination remained negative. Within a few days of infusion therapy the patient’s clinical condition significantly improved and the diagnostic imaging 4 weeks later showed complete resolution of the lesion. We diagnosed a mild encephalopathy with reversible splenial lesions (MERS type I) associated with a rotavirus infection.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85044924285&origin=inward; http://dx.doi.org/10.1007/s00112-018-0489-z; http://link.springer.com/10.1007/s00112-018-0489-z; http://link.springer.com/content/pdf/10.1007/s00112-018-0489-z.pdf; http://link.springer.com/article/10.1007/s00112-018-0489-z/fulltext.html; https://dx.doi.org/10.1007/s00112-018-0489-z; https://link.springer.com/article/10.1007/s00112-018-0489-z
Springer Science and Business Media LLC
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