Literature DB >> 154406

Histochemical and ultrastructural findings in a case of centronuclear myopathy.

L Palmucci, A Bertolotto, G Monga, G Ardizzone, D Schiffer.   

Abstract

A case of centronuclear myopathy is presented. The presence of central nuclei in almost all fibres, the existence of type I fibres only, the histochemical pattern of a negative central zone with a perinuclear halo and a hyperactive rim with oxidative enzymes and the ultrastructural data are discussed in the light of the previous literature. The possible relationships with other myopathies are taken into consideration as well as the fact that central nuclei may be a non-specific change in several conditions. Consequently centronuclear myopathy could turn out to be a syndrome from which different entities can be isolated.

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Year:  1978        PMID: 154406     DOI: 10.1159/000114970

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


  1 in total

1.  Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.

Authors:  H Sugie; R Hanson; G Rasmussen; M A Verity
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-06       Impact factor: 10.154

  1 in total

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