Literature DB >> 10463350

Electrophysiological diagnosis of motor neuron disease and pure motor neuropathy.

P Bouche1, N Le Forestier, T Maisonobe, E Fournier, J C Willer.   

Abstract

Motor neuron disease (MND) is a group of disorders in which there is degeneration of upper and lower motor neurons to a variable degree. Amyotrophic lateral sclerosis is the most frequent form of the disease, presenting with both upper and lower motor neuron involvement. Frequently, especially in the early stages of the disease, only lower motor neuron signs are present. In these conditions, some pure motor neuropathies may resemble MND. The diagnosis is of importance because some of these motor neuropathies are "dysimmune" disorders and may respond to immune therapies. In such diseases the multifocal motor neuropathy with conduction block appears to be the more frequent. In MND and pure motor neuropathies, the electrophysiological examination is the most decisive test. In MND, it is of diagnostic importance. In addition, it is useful in the assessment of disease severity and progression, in the evaluation of therapeutic trials and in the understanding of etiopathogenesis of the disease. In pure motor neuropathies, the presence of conduction block leads to immune treatment with good response in more than 50% of the cases.

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Year:  1999        PMID: 10463350     DOI: 10.1007/s004150050397

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  3 in total

1.  Peripheral (limb) myokymic discharges in motor neuron disease.

Authors:  Javeria Rauf; Junaid Akhtar; Bhojo Assumal Khealani; Liaquat Ali
Journal:  BMJ Case Rep       Date:  2012-07-30

2.  Simultaneous optical and electrical in vivo analysis of the enteric nervous system.

Authors:  Nikolai Rakhilin; Bradley Barth; Jiahn Choi; Nini L Muñoz; Subhash Kulkarni; Jason S Jones; David M Small; Yu-Ting Cheng; Yingqiu Cao; Colleen LaVinka; Edwin Kan; Xinzhong Dong; Michael Spencer; Pankaj Pasricha; Nozomi Nishimura; Xiling Shen
Journal:  Nat Commun       Date:  2016-06-07       Impact factor: 14.919

Review 3.  Clinical Mimickers of Amyotrophic Lateral Sclerosis-Conditions We Cannot Afford to Miss.

Authors:  Nishita Singh; Sucharita Ray; Achal Srivastava
Journal:  Ann Indian Acad Neurol       Date:  2018 Jul-Sep       Impact factor: 1.383

  3 in total

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