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KCNQ2 encephalopathy: Delineation of the electroclinical phenotype and treatment response
Neonatal-onset epilepsies are rare conditions, mostly genetically determined, that can have a benign or severe phenotype.(1,2) There is recent recognition of de novo KCNQ2 mutations in patients with severe neonatal-onset epilepsy with intractable seizures and severe psychomotor impairment, termed KC...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3929196/ https://ncbi.nlm.nih.gov/pubmed/24371303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000000060 |
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