Literature DB >> 1662773

Stimulated single-fiber electromyography in Lambert-Eaton myasthenic syndrome.

V Chaudhry1, D F Watson, S J Bird, D R Cornblath.   

Abstract

The Lambert-Eaton myasthenic syndrome (LEMS) is an autoimmune disorder of neuromuscular transmission. Electrodiagnosis is confirmed by an increase in compound muscle action potential amplitude during high-frequency repetitive nerve stimulation or following brief exercise. We describe the results of stimulated single-fiber electromyography in 4 patients with disorders of neuromuscular transmission: LEMS (2), LEMS/myasthenia gravis (MG) overlap (1), and MG (1). Stimulated SFEMG was performed in the extensor digitorum communis muscle with axonal intramuscular suprathreshold stimulation at low and high rates. In all 4 patients, a rate dependence of jitter was found. In LEMS and LEMS/MG, jitter and blocking improved with high stimulation rates, as compared with the opposite effect in MG. We conclude that stimulated SFEMG is a valuable technique in the diagnosis of LEMS.

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Year:  1991        PMID: 1662773     DOI: 10.1002/mus.880141215

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  3 in total

1.  Systemic effect of local botulinum toxin injections unmasks subclinical Lambert-Eaton myasthenic syndrome.

Authors:  F Erbguth; D Claus; A Engelhardt; D Dressler
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-11       Impact factor: 10.154

2.  Stimulated single-fiber electromyography (sSFEMG) in Lambert-Eaton syndrome.

Authors:  Vincenzo Todisco; Giovanni Cirillo; Rocco Capuano; Alessandro d'Ambrosio; Gioacchino Tedeschi; Antonio Gallo
Journal:  Clin Neurophysiol Pract       Date:  2018-08-13

Review 3.  Lambert-Eaton Myasthenic syndrome: early diagnosis is key.

Authors:  Trajche Ivanovski; Francesc Miralles
Journal:  Degener Neurol Neuromuscul Dis       Date:  2019-05-13
  3 in total

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