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Dysarthria and broader motor speech deficits in Dravet syndrome
OBJECTIVE: To analyze the oral motor, speech, and language phenotype in 20 children and adults with Dravet syndrome (DS) associated with mutations in SCN1A. METHODS: Fifteen verbal and 5 minimally verbal DS patients with SCN1A mutations (aged 15 months-28 years) underwent a tailored assessment batte...
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| Vydáno v: | Neurology |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Lippincott Williams & Wilkins
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5344083/ https://ncbi.nlm.nih.gov/pubmed/28148630 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000003635 |
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