Autism and behavior in adult patients with Dravet syndrome (DS)

J. J. L. Berkvens, I. Veugen, M. J. B. M. Veendrick-Meekes, F. M. Snoeijen-Schouwenaars, H. J. Schelhaas, M. H. Willemsen, I. Y. Tan*, A. P. Aldenkamp

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Introduction: Autism and behavioral characteristics in adults with Dravet syndrome (DS) have rarely been systematically studied. Method: Three scales were used to assess the outcomes of DS in adulthood in terms of autism and behavior. All the adult patients with DS, nine male and four female, aged between 18 and 60 years, living at the Epilepsy Center Kempenhaeghe in The Netherlands were included in the study. In addition, the past medical history of each patient was systematically screened for diagnoses like autism, Pervasive Development Disorder-Not Otherwise Specified (PDD-NOS), autism spectrum disorder (ASD), hyperactivity, Attention Deficit Hyperactivity Disorder (ADHD), and self-mutilation. Information concerning past and current use of psychoactive drugs was also evaluated. Results: Eight patients (61.5%) were classified as having autism spectrum disorder (ASD) according to the AVZ-R or according to the medical record. Self-mutilation was seen in four patients (30.8%), hyperactivity in none. Three patients (23.1%) currently used psychoactive drugs. Conclusion: Autism spectrum disorders persist in adult patients with DS, while certain characteristics associated with behavioral problems, such as hyperactivity or use of psychoactive medication, seem to be less prominent than in childhood.
Original languageEnglish
Pages (from-to)11-16
JournalEpilepsy & Behavior
Volume47
DOIs
Publication statusPublished - Jun 2015

Keywords

  • Dravet syndrome
  • Severe Myoclonic Epilepsy in Infancy (SMEI)
  • Adulthood
  • Behavior
  • Autism

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