Bradley D1,2, Whelan R1,2, Kimmich O1, O’Riordan S1, Mulrooney N1, Brady P1, Walsh R1, Reilly RB2, Hutchinson S1Molloy F3Hutchinson M1

 

J Neurol. 2012 Jan;259(1):77-82. doi: 10.1007/s00415-011-6125-7. Epub 2011 Jun 8

 

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1 Department of Neurology, St. Vincent’s University Hospital, Elm Park, Dublin 4, Ireland.
2 Trinity Centre for BioEngineering, Trinity College, Dublin, Ireland.
3 Department of Clinical Neurophysiology,Beaumont Hospital, Dublin, Ireland.

ABSTRACT:


Adult-onset primary torsion dystonia (AOPTD) is an autosomal dominant disorder with markedly reduced penetrance. Sensory abnormalities are present in AOPTD and also in unaffected relatives, possibly indicating nonmanifesting gene carriage (acting as an endophenotype). The temporal discrimination threshold (TDT) is the shortest time interval at which two stimuli are detected to be asynchronous. We aimed to compare the sensitivity and specificity of three different TDT tasks (visual, tactile and mixed/visual-tactile). We also aimed to examine the sensitivity of TDTs in different AOPTD phenotypes. To examine tasks, we tested TDT in 41 patients and 51 controls using visual (2 lights), tactile (non-painful electrical stimulation) and mixed (1 light, 1 electrical) stimuli. To investigate phenotypes, we examined 71 AOPTD patients (37 cervical dystonia, 14 writer’s cramp, 9 blepharospasm, 11 spasmodic dysphonia) and 8 musician’s dystonia patients. The upper limit of normal was defined as control mean ?2.5 SD. In dystonia patients, the visual task detected abnormalities in 35/41 (85%), the tactile task in 35/41 (85%) and the mixed task in 26/41 (63%); the mixed task was less sensitive than the other two (p = 0.04).


 

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