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Extraneurological sparing in long‐lived typical Lafora disease
Lafora disease (LD) clinically appears in previously healthy teenagers as progressively worsening seizures, myoclonus, dementia, and ultimately a vegetative state leading to death within a decade of its onset. Here we present a typical case of LD in which the patient survived until the age of 40. Al...
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| Veröffentlicht in: | Epilepsia Open |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
John Wiley and Sons Inc.
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5983108/ https://ncbi.nlm.nih.gov/pubmed/29881811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/epi4.12224 |
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