Propriospinal myodonus after treatment with ciprofloxacin

The clinical and electrophysiological features of a truncal myoclonus in a 55-year-old man are described. The electromyographic characteristics point toward propriospinal myoclonus. It is suggested that a myoclonic generator was released after use of ciprofloxacin. by antagonising the gamma-aminobutyric acid metabolism. (C) 2004 Movement Disorder Society

Dystonic neck muscles show a shift in relative autospectral power during isometric contractions

ObjectiveTo identify effects of a deviant motor drive in the autospectral power of dystonic muscles during voluntary contraction in cervical dystonia patients.MethodsSubmaximal (20%) isometric head-neck tasks were performed with the head fixed, measuring surface EMG of the sternocleidomastoid, splenius capitis and semispinalis capitis in CD patients and controls. Autospectral power of muscle activity, and head forces was analyzed using cumulative distribution functions (CDF). A downward shift between the theta/low alpha-band (3-10 Hz) and the high alpha/beta-band (10-30 Hz) was detected using the CDF10, defined as the cumulative power from 3-10 Hz relative to power from 3-30 Hz.ResultsCDF10 was increased in dystonic muscles compared to controls and patient muscles unaffected by dystonia, due to a 3-10 Hz power increase and a 10-30 Hz decrease. CDF10 also increased in patient head forces.ConclusionsSubmaximal isometric contractions with the head fixed provided a well-defined test condition minimizing effects of reflexive feedback and tremor. We associate shifts in autospectral power with prokinetic sensorimotor control.SignificanceAnalysis of autospectral power in isometric tasks with the head fixed is a promising approach in research and diagnostics of cervical dystonia.Biomechatronics & Human-Machine ControlIntelligent Vehicle

Hereditary myoclonus-dystonia associated with epilepsy

A five-generation Dutch family with inherited myoclonus-dystonia (M-D) is described. Genetic analysis revealed a novel truncating mutation within the epsilon-sarcoglycan gene (SGCE). In three of five gene carriers, epilepsy and/or EEG abnormalities were associated with the symptoms of myoclonus and dystonia. The genetic and clinical heterogeneity of M-D is extended. EEG changes and epilepsy should not be considered exclusion criteria for the clinical diagnosis of M-D

Dynamic head-neck stabilization in cervical dystonia

Background Effective sensorimotor integration is essential to modulate (adapt) neck stabilization strategies in response to varying tasks and disturbances. This study evaluates the hypothesis that relative to healthy controls cervical dystonia patients have an impaired ability to modulate afferent feedback for neck stabilization with changes in the frequency content of mechanical perturbations. Methods We applied anterior-posterior displacement perturbations (110 s) on the torso of seated subjects, while recording head-neck kinematics and muscular activity. We compared low bandwidth (0.2–1.2 Hz) and high bandwidth (0.2–8 Hz) perturbations where our previous research showed a profound modulation of stabilization strategies in healthy subjects. Cervical dystonia patients and age matched controls performed two tasks: (1) maintain head forward posture and (2) allow dystonia to dictate head posture. Findings Patients and controls demonstrated similar kinematic and muscular responses. Patient modulation was similar to that of healthy controls (P > 0.05); neck stiffness and afferent feedback decreased with high bandwidth perturbations. During the head forward task patients had an increased neck stiffness relative to controls (P Accepted Author ManuscriptBiomechatronics & Human-Machine ControlIntelligent Vehicle