| Literature DB >> 31256146 |
Ellen van der Plas1, Robin Schubert2, Ralf Reilmann2,3,4, Peggy C Nopoulos1.
Abstract
Q-Motor is utilized across various clinical trials in adults with Huntington's disease (HD) to provide quantitative, reliable assessments of motor abilities. With gene-knockdown therapies entering the clinic, development of preventative therapies for pediatric carriers of the HD mutation seems imminent. It is currently unclear if Q-Motor is useful for tracking changes in motor abilities in pediatric HD patients or at-risk youth, as most assessments have never been administered in children. We demonstrate the feasibility of administering Q-Motor tasks in a sample of children recruited from the community, and we show that Q-Motor is sensitive to age-related changes in motor abilities.Entities:
Keywords: Huntington’s disease; Q-Motor; adolescents; children; development; endpoint; motor
Mesh:
Year: 2019 PMID: 31256146 DOI: 10.3233/JHD-190353
Source DB: PubMed Journal: J Huntingtons Dis ISSN: 1879-6397