## Abstract A 48‐year‐old man with severe, lifelong Tourette's syndrome (TS) characterized by forceful self‐injurious motor tics and obsessive‐compulsive disorder was treated with bilateral deep brain stimulation (DBS). The decision to treat was based on his progressive neurological impairment (lef
Deep Brain Stimulation in Tourette’s Syndrome
✍ Scribed by Linda Ackermans; Yasin Temel; Veerle Visser-Vandewalle
- Book ID
- 104072042
- Publisher
- Springer-Verlag
- Year
- 2008
- Tongue
- English
- Weight
- 78 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1933-7213
No coin nor oath required. For personal study only.
✦ Synopsis
Tourette's Syndrome (TS) is a neuropsychiatric disorder characterized by motor and vocal tics, often associated with behavioral disorders. Symptoms often disappear before or during adulthood. The pathophysiology of TS is still a matter of considerable debate. Current knowledge of cortico-basal ganglia-thalamocortical circuits provide explanations for the beneficial effects of deep brain stimulation (DBS) on tics. When conservative treatment fails in patients with severe TS, DBS may be a therapeutic option. In 1999, thalamic DBS was introduced for intractable TS. Since then, multiple targets have been used in a small number of patients, including the globus pallidus pars interna and the nucleus accumbens. Inclusion and exclusion criteria have been formulated to identify good candidates for DBS.
📜 SIMILAR VOLUMES
In this report, we describe the effects of bilateral thalamic stimulation in one patient and of bilateral pallidal stimulation in another patient. Both patients suffered from
Typical attack elicited by holding a weight in the right arm. After only a few seconds, myoclonic jerks affecting the right arm, predominantly the index finger and thumb, and some additional dystonic posturing of the right arm appear, exceeding the actual holding of the object.