Sporadic rapid-onset dystonia–parkinsonism syndrome: Failure of bilateral pallidal stimulation
✍ Scribed by Angela Deutschländer; Friedrich Asmus; Thomas Gasser; Ulrich Steude; Kai Bötzel
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 61 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We report on a woman who had a severe sporadic nonprogressive dystonia–parkinsonism syndrome with rapid onset of symptoms at age 21. Secondary causes for dystonia were ruled out. No response to levodopa/carbidopa was seen. The patient fulfilled all diagnostic criteria of rapid‐onset dystonia–parkinsonism, except for autosomal‐dominant inheritance. Bilateral deep brain stimulation of the globus pallidus failed to alleviate her symptoms. © 2004 Movement Disorder Society
📜 SIMILAR VOLUMES
## Abstract “Lubag” or X‐linked dystonia‐parkinsonism (XDP) is a genetic syndrome afflicting Filipino men. Intracranial surgical procedures for Lubag have been unsuccessful. We report a 45‐year‐old Filipino male with genetically confirmed XDP who underwent bilateral pallidal deep brain stimulation