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Epilepsy and the natural history of Rett syndrome
BACKGROUND: Rett syndrome (RTT) is a neurodevelopmental disorder primarily seen in females, most with a mutation in MECP2. Epilepsy has been reported in 50%–80%. Previous reports were based on small sample sizes or parent-completed questionnaires, or failed to consider the impact of specific MECP2 m...
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| Main Authors: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Academy of Neurology
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2836870/ https://ncbi.nlm.nih.gov/pubmed/20231667 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181d6b852 |
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