Primary lateral sclerosis: Clinical and laboratory features in 25 patients

Mike A. Singer, Suleiman Kojan, Richard J. Barohn, Laura Herbelin, Sharon P. Nations, Jaya R. Trivedi, Carlayne E Jackson, Dennis K. Burns, Philip J. Boyer, Gil I. Wolfe

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Objective: The objective of this study was to characterize the clinical features and natural history of primary lateral sclerosis (PJLS). Background: PLS is a motor neuron disorder defined by corticospinal and corticobulbar tract dysfunction without clinically significant lower motor neuron involvement. Methods: We collected data from 25 patients with PLS seen in 2 academic neurology departments over a 5-year period. Results: The PLS population represented approximately 3% of acquired motor neuron disease cases seen during that period. Twenty-three patients (92%) presented with lower limb weakness, spasticity, or difficulty with ambulation. None presented with upper limb symptoms. Eleven patients (44%) developed bulbar symptoms. All patients had hyperreflexia and increased muscle tone. Muscle weakness was observed in 15 patients (60%) and tended to be mild and asymmetric. Needle electromyography (EMG) was normal or showed only fasciculations in 15 patients (60%); 10 patients had features of mild active denervation, consisting of fibrillation or positive sharp wave potentials, but the extent of these findings did not satisfy World Federation of Neurology electropliysiological criteria for the diagnosis of amyotrophic lateral sclerosis. Fourteen patients (52%) continued independent ambulation. Of the 10 patients with active denervation on EMG, 6 (60%) required a walker, scooter, or wheelchair at a mean follow up of 6.2 years. There were no fatalities over the 5-year period. Conclusions: Our experience supports the observation that PLS progresses more slowly than other forms of acquired motor neuron disease, particularly amyotrophic lateral sclerosis. Follow-up data suggest that patients with active denervation changes develop greater disability.

Original languageEnglish (US)
Pages (from-to)1-9
Number of pages9
JournalJournal of Clinical Neuromuscular Disease
Volume7
Issue number1
DOIs
StatePublished - Sep 2005

Fingerprint

Motor Neuron Disease
Denervation
Pyramidal Tracts
Amyotrophic Lateral Sclerosis
Electromyography
Motor Neurons
Muscle Hypertonia
Fasciculation
Mobility Limitation
Abnormal Reflexes
Wheelchairs
Muscle Weakness
Neurology
Upper Extremity
Walking
Needles
Lower Extremity

Keywords

  • Electromyography
  • Motor neuron disease
  • Primary lateral sclerosis

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Singer, M. A., Kojan, S., Barohn, R. J., Herbelin, L., Nations, S. P., Trivedi, J. R., ... Wolfe, G. I. (2005). Primary lateral sclerosis: Clinical and laboratory features in 25 patients. Journal of Clinical Neuromuscular Disease, 7(1), 1-9. https://doi.org/10.1097/01.cnd.0000176974.61136.45

Primary lateral sclerosis : Clinical and laboratory features in 25 patients. / Singer, Mike A.; Kojan, Suleiman; Barohn, Richard J.; Herbelin, Laura; Nations, Sharon P.; Trivedi, Jaya R.; Jackson, Carlayne E; Burns, Dennis K.; Boyer, Philip J.; Wolfe, Gil I.

In: Journal of Clinical Neuromuscular Disease, Vol. 7, No. 1, 09.2005, p. 1-9.

Research output: Contribution to journalArticle

Singer, MA, Kojan, S, Barohn, RJ, Herbelin, L, Nations, SP, Trivedi, JR, Jackson, CE, Burns, DK, Boyer, PJ & Wolfe, GI 2005, 'Primary lateral sclerosis: Clinical and laboratory features in 25 patients', Journal of Clinical Neuromuscular Disease, vol. 7, no. 1, pp. 1-9. https://doi.org/10.1097/01.cnd.0000176974.61136.45
Singer, Mike A. ; Kojan, Suleiman ; Barohn, Richard J. ; Herbelin, Laura ; Nations, Sharon P. ; Trivedi, Jaya R. ; Jackson, Carlayne E ; Burns, Dennis K. ; Boyer, Philip J. ; Wolfe, Gil I. / Primary lateral sclerosis : Clinical and laboratory features in 25 patients. In: Journal of Clinical Neuromuscular Disease. 2005 ; Vol. 7, No. 1. pp. 1-9.
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