Literature DB >> 6685835

Motor neuron disease (ALS): evaluation of detection thresholds of cutaneous sensation.

D W Mulder, W Bushek, E Spring, J Karnes, P J Dyck.   

Abstract

Cutaneous touch-pressure, vibration, and thermal cooling detection thresholds were estimated on the skin of one foot for 80 patients with motor neuron disease (MND) and compared with that of more than 300 site, age, and sex-matched healthy controls. Fourteen of the patients had elevated thresholds (greater than or equal to 95th percentile): 7 showed elevated thresholds of sensitive points, 5 an increased number of insensitive grid points, and 2 a combination of these criteria. Therefore, raised vibration thresholds occur more frequently in MND patients than in controls (p less than 0.001). A detection threshold abnormality was not demonstrated for touch-pressure or for thermal cooling. These results are in keeping with the demonstrated increased cutaneous myelinated fiber degeneration in this condition and with evidence of sensory neural system involvement at postmortem examination. Although motor neurons are selectively vulnerable in MND, afferent neurons may also be affected, albeit less frequently and/or to a lesser degree.

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Year:  1983        PMID: 6685835     DOI: 10.1212/wnl.33.12.1625

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  8 in total

Review 1.  Motor neuron disease.

Authors:  M Swash
Journal:  Postgrad Med J       Date:  1992-07       Impact factor: 2.401

2.  Selective and asymmetric vulnerability of corticospinal and spinocerebellar tracts in motor neuron disease.

Authors:  M Swash; C L Scholtz; G Vowles; D A Ingram
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-06       Impact factor: 10.154

3.  Progressive sensory nerve dysfunction in amyotrophic lateral sclerosis: a prospective clinical and neurophysiological study.

Authors:  R Gregory; K Mills; M Donaghy
Journal:  J Neurol       Date:  1993-05       Impact factor: 4.849

4.  Sensory involvement in motor neuron disease: further evidence from automated thermal threshold determination.

Authors:  G A Jamal; A I Weir; S Hansen; J P Ballantyne
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-09       Impact factor: 10.154

5.  Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study.

Authors:  K Pugdahl; A Fuglsang-Frederiksen; M de Carvalho; B Johnsen; P R W Fawcett; A Labarre-Vila; R Liguori; W A Nix; I S Schofield
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-07       Impact factor: 10.154

6.  A mouse model of pharyngeal dysphagia in amyotrophic lateral sclerosis.

Authors:  Teresa E Lever; Emmanuelle Simon; Kathleen T Cox; Norman F Capra; Kevin F O'Brien; Monica S Hough; Alexander K Murashov
Journal:  Dysphagia       Date:  2009-06-03       Impact factor: 3.438

7.  Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis.

Authors:  Brandie R Morgan; Joan R Coates; Gayle C Johnson; G Diane Shelton; Martin L Katz
Journal:  J Neurosci Res       Date:  2013-12-21       Impact factor: 4.164

8.  Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI study.

Authors:  Chunyan Luo; Qin Chen; Rui Huang; Xueping Chen; Ke Chen; Xiaoqi Huang; HeHan Tang; Qiyong Gong; Hui-Fang Shang
Journal:  PLoS One       Date:  2012-09-20       Impact factor: 3.240

  8 in total

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