Literature DB >> 24862941

Neuromuscular junction disorders mimicking myopathy.

Phillip C Mongiovi1, Bakri Elsheikh, Victoria H Lawson, John T Kissel, W David Arnold.   

Abstract

INTRODUCTION: Small-amplitude, short-duration motor unit action potentials are non-specific findings seen in myopathies and neuromuscular junction (NMJ) disorders. NMJ studies (repetitive nerve stimulation and single-fiber electromyography) can determine if such findings are related to NMJ abnormalities but are not considered routinely in atypical cases.
METHODS: Medical records of 338 patients with confirmed NMJ disorders were reviewed to identify cases with a clinical or electrodiagnostic impression of myopathy during initial evaluation. A history of muscle biopsy with findings that did not support a myopathic process was required for inclusion.
RESULTS: Four patients met the inclusion criteria. NMJ studies were abnormal in all cases. One patient had elevated acetylcholine receptor antibodies. Three patients were antibody negative: 2 demonstrated immunotherapy responsiveness, and 1 had a Rapsyn mutation.
CONCLUSIONS: NMJ disorders may mimic myopathies, and NMJ studies should be performed to clarify so-called "myopathic" electromyographic findings to avoid unnecessary testing and delayed diagnosis.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  action potentials; electromyography; myasthenia gravis; neuromuscular junction disorders; repetitive nerve stimulation

Mesh:

Substances:

Year:  2014        PMID: 24862941      PMCID: PMC4512737          DOI: 10.1002/mus.24300

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


  7 in total

1.  Brief, small, abundant motor-unit action potentials. A further critique of electromyographic interpretation.

Authors:  W K Engel
Journal:  Neurology       Date:  1975-02       Impact factor: 9.910

2.  Open-biopsy electromyography. Direct correlation of a pattern of excessively recruited, pathologically small motor unit potentials with histologic evidence of neuropathy.

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Journal:  Arch Neurol       Date:  1979-07

3.  The description of motor unit potentials in electromyography.

Authors:  J R Daube
Journal:  Neurology       Date:  1978-07       Impact factor: 9.910

4.  Assessment of variability in the shape of the motor unit action potential, the "jiggle," at consecutive discharges.

Authors:  E V Stålberg; M Sonoo
Journal:  Muscle Nerve       Date:  1994-10       Impact factor: 3.217

5.  Difference in distribution of muscle weakness between myasthenia gravis and the Lambert-Eaton myasthenic syndrome.

Authors:  P W Wirtz; M Sotodeh; M Nijnuis; P A Van Doorn; B G M Van Engelen; R Q Hintzen; P L M De Kort; J B Kuks; A Twijnstra; M De Visser; L H Visser; J H Wokke; A R Wintzen; J J Verschuuren
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-12       Impact factor: 10.154

6.  Inclusion body myositis mimicking motor neuron disease.

Authors:  R Dabby; D J Lange; W Trojaborg; A P Hays; R E Lovelace; T H Brannagan; L P Rowland
Journal:  Arch Neurol       Date:  2001-08

7.  Congenital myasthenic syndromes in childhood: diagnostic and management challenges.

Authors:  M Kinali; D Beeson; M C Pitt; H Jungbluth; A K Simonds; A Aloysius; H Cockerill; T Davis; J Palace; A Y Manzur; C Jimenez-Mallebrera; C Sewry; F Muntoni; S A Robb
Journal:  J Neuroimmunol       Date:  2008-08-15       Impact factor: 3.478

  7 in total
  1 in total

1.  Ischemic stroke-induced polyaxonal innervation at the neuromuscular junction is attenuated by robot-assisted mechanical therapy.

Authors:  Maria H H Balch; Hallie Harris; Deepti Chugh; Surya Gnyawali; Cameron Rink; Shahid M Nimjee; W David Arnold
Journal:  Exp Neurol       Date:  2021-05-25       Impact factor: 5.620

  1 in total

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