Literature DB >> 7094950

Myasthenic neuromyopathy. An unusual neuromuscular disorder.

M Kinoshita, H Nakazato, N Wakata, E Satoyoshi.   

Abstract

4 cases with an identical neuromuscular disorder are presented. The disorder was characterized by slowly progressive weakness and wasting of the proximal muscles together with either ocular or bulbar symptoms, fatigability, positive tensilon test, myasthenic response on repetitive nerve stimulations, elevated serum creatine phosphokinase, and neuropathic and myopathic muscle pathology. All the patients showed a fairly good response to anti-ChE medications and steroid administration. Serum creatine phosphokinase levels returned to normal values after steroid therapy. Myasthenia, polymyositis or other neuromuscular disorders were discussed in the differential diagnosis.

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Year:  1982        PMID: 7094950     DOI: 10.1159/000115454

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  2 in total

1.  Congenital myopathy with myasthenic features and congenital cataract in two siblings.

Authors:  Y Nishida; T Kobayashi; M Machi; T Yamada; T Kitaguchi; K Oda; I Goto
Journal:  J Neurol       Date:  1989-03       Impact factor: 4.849

2.  Adult-onset Satoyoshi syndrome and response to plasmapheresis.

Authors:  Rajeshwari Aghoram; P R Srijithesh; Sudheeran Kannoth
Journal:  Ann Indian Acad Neurol       Date:  2016 Jan-Mar       Impact factor: 1.383

  2 in total

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