Literature DB >> 954775

Congenital non-progressive myopathy with type II fibre atrophy and internal nuclei.

R Scelsi, G Lanzi, L Nespoli, P Poggi.   

Abstract

A particular form of congenital non-progressive myopathy in a 5-year-old boy is described. The morphological features include predominant atrophy and rarity of type II muscle fibres, internally placed nuclei and myofibrillar degeneration in affected fibres.

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Year:  1976        PMID: 954775     DOI: 10.1159/000114750

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


  2 in total

1.  Patterns of neuromuscular disease. As related to stages of normal embryogenesis in voluntary muscle.

Authors:  A Korényi-Both; G Marosán
Journal:  Am J Pathol       Date:  1979-05       Impact factor: 4.307

2.  Pleocore disease. Multi-minicore disease and focal loss of cross striations.

Authors:  J J Martin; M Bruyland; H F Busch; J P Farriaux; I Krivosic; C Ceuterick
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

  2 in total

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