ADVANCED TREATMENTS IN DYSTONIA Marie VIDAILHET, Sorbonne Université, Institut du
Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, AP-HP, Hôpital Salpetriere, Paris,
France Therapeutic strategy for dystonia can be approached in two ways: based on etiology
and pathophysiology, which concerns a small number of diseases and syndromes among
which some paroxysmal dystonias/abnormal movements (Glut 1 deficiency), rare genetic
forms (ADCY5, L-Dopa sensitive dystonia) or diseases in which dystonia is one of the
multiple clinical expressions (Wilson) or based on phenomenology and dystonia severity.
In most cases, the treatment is mainly symptomatic and based on a single or combined
approach with botulinum toxin-kinesitherapy/medications/deep brain stimulation. Although
a long experience is being acquired with long term follow-up results. Therapeutic
advances are being made as a result of new pathophysiological, imaging or physiological
data, technological developments (DBS, FUS) or a better definition of the objectives
and a more complete evaluation of the results, taking into account not only the motor
signs but also the non-motor signs. Moreover, teams experience has expanded over the
year, from pediatric forms to the long-term effects of parties who combine very long
follow-up periods, with the consideration of age and long-term effects of treatments.
These different elements will be discussed with clinical cases and take home messages.
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