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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

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✦ 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


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First case of X-linked dystonia-parkinso
✍ Virgilio Gerald H. Evidente; Mark K. Lyons; Mark Wheeler; Renee Hillman; Luann H 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB

## 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