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Uncommon mutation in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)
A 26-year-old man presented to the emergency department with new-onset generalised tonic–clonic seizures. His clinical picture suggested either autoimmune or infectious encephalitis while his brain imaging raised the possibility of a stroke. A detailed developmental and childhood medical history add...
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| Vydáno v: | BMJ Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5337635/ https://ncbi.nlm.nih.gov/pubmed/28242802 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2016-218133 |
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