Source:Clinical Neurophysiology, Volume 129, Issue 7
Author(s): Stefanie Schreiber, Frank Schreiber, Grazyna Debska-Vielhaber, Cornelia Garz, Nathalie Hensiek, Judith Machts, Susanne Abdulla, Reinhard Dengler, Susanne Petri, Peter J. Nestor, Stefan Vielhaber
ObjectiveWe aimed to assess whether differential peripheral nerve involvement parallels dissociated forearm muscle weakness in amyotrophic lateral sclerosis (ALS).MethodsThe analysis comprised 41 ALS patients and 18 age-, sex-, height- and weight-matched healthy controls. Strength of finger-extension and -flexion was measured using the Medical Research Council (MRC) scale. Radial, median and ulnar nerve sonographic cross-sectional area (CSA) and echogenicity, expressed by the hypoechoic fraction (HF), were determined.ResultsIn ALS, finger extensors were significantly weaker than finger flexors. Sonographic evaluation revealed peripheral nerve atrophy, affecting various nerve segments in ALS. HF was unaltered.ConclusionsThis systematic study confirmed a long-observed physical examination finding in ALS – weakness in finger-extension out of proportion to finger-flexion. This phenomenon was not related to any particular sonographic pattern of upper limb peripheral nerve alteration.SignificanceIn ALS, dissociated forearm muscle weakness could aid in the disease's diagnosis. Nerve ultrasound did not provide additional information on the differential involvement of finger-extension and finger-flexion strength.
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