Literature DB >> 28148630

Dysarthria and broader motor speech deficits in Dravet syndrome.

Samantha J Turner1, Amy Brown1, Marta Arpone1, Vicki Anderson1, Angela T Morgan1, Ingrid E Scheffer2.   

Abstract

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 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.
© 2017 American Academy of Neurology.

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Year:  2017        PMID: 28148630      PMCID: PMC5344083          DOI: 10.1212/WNL.0000000000003635

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


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