| Literature DB >> 11009215 |
L Angelini1, N Nardocci, M Estienne, C Conti, I Dones, G Broggi.
Abstract
We report a 13-year-old boy who developed severe, refractory dystonia-dyskinesias as an abrupt worsening of a previously nonprogressive movement disorder. The movements became continuous, requiring artificial respiration and continuous sedation in the intensive-care unit. Various drugs and drug combinations failed to achieve control. The child was then treated successfully with bilateral pallidal (GPi) stimulation as shown in the videotape. Four months later and without medication, the boy regained autonomous gait and audible speech; his neurologic condition continues to improve.Entities:
Mesh:
Year: 2000 PMID: 11009215 DOI: 10.1002/1531-8257(200009)15:5<1010::aid-mds1039>3.0.co;2-5
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338