Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16659
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dc.contributor.authorTurner, Samantha J-
dc.contributor.authorBrown, Amy-
dc.contributor.authorArpone, Marta-
dc.contributor.authorAnderson, Vicki-
dc.contributor.authorMorgan, Angela T-
dc.contributor.authorScheffer, Ingrid E-
dc.date2017-02-21-
dc.date.accessioned2017-05-26T05:45:11Z-
dc.date.available2017-05-26T05:45:11Z-
dc.date.issued2017-02-21-
dc.identifier.citationNeurology 2017; 88(8): 743-749en_US
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/16659-
dc.description.abstractOBJECTIVE: 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 battery. RESULTS: Speech was characterized by imprecise articulation, abnormal nasal resonance, voice, and pitch, and prosody errors. Half of verbal patients had moderate to severely impaired conversational speech intelligibility. Oral motor impairment, motor planning/programming difficulties, and poor postural control were typical. Nonverbal individuals had intentional communication. Cognitive skills varied markedly, with intellectual functioning ranging from the low average range to severe intellectual disability. Language impairment was congruent with cognition. CONCLUSIONS: We describe a distinctive speech, language, and oral motor phenotype in children and adults with DS associated with mutations in SCN1A. Recognizing this phenotype will guide therapeutic intervention in patients with DS.en_US
dc.subjectDysarthriaen_US
dc.subjectEpilepsies, Myoclonicen_US
dc.subjectDyskinesiasen_US
dc.titleDysarthria and broader motor speech deficits in Dravet syndromeen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleNeurologyen_US
dc.identifier.affiliationDepartment of Paediatrics, The University of Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Psychology, The Royal Children's Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationNeuroscience of Speech Group, Clinical Sciences Theme, Murdoch Childrens Research Institute, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationAustralian Centre for Child Neuropsychological Studies, Murdoch Childrens Research Institute, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationFlorey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28148630en_US
dc.identifier.doi10.1212/WNL.0000000000003635en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-2311-2174en_US
dc.type.austinJournal Articleen_US
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeJournal Article-
crisitem.author.deptEpilepsy Research Centre-
Appears in Collections:Journal articles
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