Toward a more personalized motor function rehabilitation in Myotonic dystrophy type 1: The role of neuroplasticity.
Ontology highlight
ABSTRACT: Myotonic dystrophy type 1 (DM1) is the most prevalent adult muscular dystrophy, often accompanied by impairments in attention, memory, visuospatial and executive functions. Given that DM1 is a multi-system disorder, it requires a multi-disciplinary approach, including effective rehabilitation programs, focusing on the central nervous system neuroplasticity, in order to develop patient-tailored rehabilitative procedures for motor function recovery. Herein, we performed a transcranial magnetic stimulation (TMS) study aimed at investigating central motor conduction time, sensory-motor plasticity, and cortical excitability in 7 genetically defined DM1 patients. As compared to healthy individuals, DM1 patients showed a delayed central motor conduction time and an abnormal sensory-motor plastici
SUBMITTER: Portaro S
PROVIDER: S-EPMC5444819 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature
ACCESS DATA