Literature DB >> 2816279

Adult-onset centronuclear myopathy: evidence against a neurogenic pathology.

A Baradello1, G Vita, P Girlanda, M L Roberto, G Carrozza.   

Abstract

A case of sporadic adult-onset centronuclear myopathy is presented. EMG was myopathic and nerve conduction study entirely normal. Single-fiber electromyography showed a normal percentage of potential pairs with abnormal jitter, slightly increased mean jitter value, no blocking and normal fiber density. Somatosensory and motor evoked potentials were within the normal limits. While it is still a subject of debate whether centronuclear myopathy is neuropathic or myopathic in origin, our findings are against peripheral nerve and CNS involvement.

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Year:  1989        PMID: 2816279     DOI: 10.1111/j.1600-0404.1989.tb03860.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  3 in total

1.  Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia.

Authors:  Teerin Liewluck; Xin-Ming Shen; Margherita Milone; Andrew G Engel
Journal:  Neuromuscul Disord       Date:  2011-04-08       Impact factor: 4.296

Review 2.  Current status of the congenital myasthenic syndromes.

Authors:  Andrew G Engel
Journal:  Neuromuscul Disord       Date:  2011-11-21       Impact factor: 4.296

Review 3.  Congenital myasthenic syndromes in 2012.

Authors:  Andrew G Engel
Journal:  Curr Neurol Neurosci Rep       Date:  2012-02       Impact factor: 5.081

  3 in total

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