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Acute encephalopathy in familial hemiplegic migraine with ATP1A2 mutation
Familial hemiplegic migraine is a rare subtype of migraine with aura which includes motor weakness. A 32-year-old woman with known familial hemiplegic migraine (point mutation in Exon 22 of the ATP1A2 gene) presented with an acute confusional state, after an initially typical migraine. On examinatio...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3702875/ https://ncbi.nlm.nih.gov/pubmed/23761507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2013-009750 |
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