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   <subfield code="a">Basal ganglia hyperechogenicity does not distinguish between patients with primary dystonia and healthy individuals</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Johann Hagenah, Inke König, Charlotte Kötter, Günter Seidel, Christine Klein, Norbert Brüggemann]</subfield>
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   <subfield code="a">Transcranial sonography (TCS) of the basal ganglia is a non-invasive tool to study movement disorders. Very few studies have addressed the question of whether TCS may detect specific echofeatures in patients with primary dystonia. The basal ganglia including the substantia nigra (SN) and the ventricular system were investigated by TCS in 84 primary dystonia patients and 43 neurologically healthy controls. Any hyperechogenicity of the lenticular nucleus was present in 57.5% of the patients and in 50.0% of the controls (p=0.453). While marked hyperechogenicity was more frequently present in the patients (17.8 vs. 7.9%), this difference was not significant (p=0.227). No differences in the occurrence of hyperechogenicity were detectable either in the caudate nucleus (21.6 vs. 39.5%, p=0.122) or the thalamus (4.1 vs. 0%, p=0.199). Marked hyperechogenicity of the caudate nucleus was rare in dystonia (4.1%) and absent in controls. There was no relationship between the side of basal ganglia hyperechogenicity and the clinically affected side of cervical dystonia. The area of SN echogenicity was similar in patients and controls (0.19±0.14 vs. 0.20±0.13cm2), but correlated negatively with increasing disease duration in the dystonia patients (ρ=-0.257, p=0.028). Width of the third ventricle correlated with increasing age (ρ=0.511, p=0.000) and, in patients, with disease duration (ρ=0.244, p=0.034) and severity of cervical dystonia (ρ=0.281, p=0.038). No characteristic abnormalities were found in the basal ganglia of primary dystonia patients. It remains to be explored whether this is due to a true absence of signal alterations in the basal ganglia of dystonia patients or to limitations of the current technology used.</subfield>
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   <subfield code="a">Springer-Verlag, 2010</subfield>
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   <subfield code="a">Dystonia</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Movement disorder</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Substantia nigra</subfield>
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   <subfield code="a">Lenticular nucleus</subfield>
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   <subfield code="a">Basal ganglia</subfield>
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   <subfield code="a">Transcranial sonography</subfield>
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   <subfield code="a">Echogenicity</subfield>
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   <subfield code="a">Hagenah</subfield>
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   <subfield code="u">Section of Clinical and Molecular Neurogenetics, University of Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Germany</subfield>
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   <subfield code="u">Department of Neurology, University of Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Germany</subfield>
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