## Abstract No consistent cerebral anatomical abnormality has ever been reported in primary focal hand dystonia (FHD). The present voxelโbased morphometry study showed a significant bilateral increase in gray matter in the hand representation area of primary somatosensory and, to a lesser extent, p
Morphometric changes of sensorimotor structures in focal dystonia
โ Scribed by Mark Obermann; Ozguer Yaldizli; Armin De Greiff; Martin Lenard Lachenmayer; Anna Rebecca Buhl; Felicitus Tumczak; Elke Ruth Gizewski; Hans-Christoph Diener; Matthias Maschke
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 202 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0885-3185
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โฆ Synopsis
Abstract
Idiopathic cervical dystonia (CD) and benign essential blepharospasm (BEB) are the most common forms of focal dystonia. Previous autopsy and imaging studies suggested that these disorders are not accompanied by structural brain abnormalities. However, recent brain voxelโbased morphometry (VBM) studies of these conditions suggest that there actually may be changes in gray matter. The objective of this stdy was to detect possible gray matter abnormalities in patients with CD and BEB using VBM and to compare the results between the two conditions and with ageโ and genderโmatched controls. Highโresolution MRI was employed to evaluate healthy controls and individuals with BEB and CD. Eleven BEB, 9 CD, and 14 healthy control subjects were imaged. VBM revealed alterations of gray matter structures involved in sensorimotor processing in the individuals with focal dystonia. In CD subjects there was increased gray matter in the thalamus, caudate head bilaterally, superior temporal lobe, and left cerebellum, while gray matter was decreased in the putamen bilaterally. BEB subjects had increased gray matter in the caudate head and cerebellum bilaterally as well as decrease in the putamen and thalamus bilaterally. These findings strongly underline the recent notion that idiopathic focal dystonias might have a detectable structural correlate. They also demonstrate structural similarities of the investigated focal dystonias, possibly reflecting a shared common pathophysiological origin. ยฉ 2007 Movement Disorder Society
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