Literature DB >> 14076166

LIGHT AND ELECTRON MICROSCOPIC STUDIES OF "MYOGRANULES" IN A CHILD WITH HYPOTONIA AND MUSCLE WEAKNESS.

P E CONEN, E G MURPHY, W L DONOHUE.   

Abstract

Examination by light and electron microscopy of more than 100 muscle biopsies revealed one very unusual case. A 4-year-old boy with non-progressive muscle weakness and hypotonia was found to have small particles, termed "myogranules", in many muscle fibres from two gastrocnemius biopsies. Paraffin sections and thin sections of plastic-embedded muscle showed that the rod-shaped myogranules measured between 0.1 and 5 microns in length, and were usually orientated in the long axis of the fibre. Normal cross-striations could not be seen in areas occupied by myogranules, although adjacent parts of the same fibre were normal. Electron micrographs showed myofilaments running through the myogranules and a periodicity similar to sections of recrystallized muscle protein paramyosin. It is possible that this child has a disturbance of muscle proteins.

Entities:  

Keywords:  BIOPSY; CHILD; MICROSCOPY, ELECTRON; MUSCULAR DISEASES

Mesh:

Substances:

Year:  1963        PMID: 14076166      PMCID: PMC1921896     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  2 in total

1.  Deletion of Y chromosome in a family with muscular dystrophy and hypospadias.

Authors:  S MULDAL; C H OCKEY
Journal:  Br Med J       Date:  1962-02-03

2.  The future of the 'floppy infant': a follow-up study of 133 patients.

Authors:  R S PAINE
Journal:  Dev Med Child Neurol       Date:  1963-04       Impact factor: 5.449

  2 in total
  27 in total

1.  Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene.

Authors:  Sylvia L Anderson; Josef Ekstein; Mary C Donnelly; Erin M Keefe; Nicole R Toto; Lauretta A LeVoci; Berish Y Rubin
Journal:  Hum Genet       Date:  2004-06-23       Impact factor: 4.132

Review 2.  Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.

Authors:  K N North; N G Laing; C Wallgren-Pettersson
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

3.  Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).

Authors:  Nigel G Laing; Danielle E Dye; Carina Wallgren-Pettersson; Gabriele Richard; Nicole Monnier; Suzanne Lillis; Thomas L Winder; Hanns Lochmüller; Claudio Graziano; Stella Mitrani-Rosenbaum; Darren Twomey; John C Sparrow; Alan H Beggs; Kristen J Nowak
Journal:  Hum Mutat       Date:  2009-09       Impact factor: 4.878

4.  Nemaline bodies in spinal progressive muscular atrophy. An autopsy case.

Authors:  H Konno; Y Iwasaki; T Yamamoto; T Inosaka
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

5.  [The diagnostic specificity of nemaline-structures].

Authors:  F Jerusalem; H Goetze; M Mumenthaler
Journal:  Z Neurol       Date:  1971

6.  [Study of a new observation of "nemaline myopathy". II. Ultrastructural findings].

Authors:  M Fardeau
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

7.  The ultrastructural morphology of the muscle fiber in myotonic dystrophy.

Authors:  J M Schröder; R D Adams
Journal:  Acta Neuropathol       Date:  1968-04-08       Impact factor: 17.088

8.  Anaesthetic implications of nemaline rod myopathy.

Authors:  M Cunliffe; F A Burrows
Journal:  Can Anaesth Soc J       Date:  1985-09

9.  Nemaline myopathy: histological, histochemical and ultrastructural studies.

Authors:  N Fukuhara; T Yuasa; T Tsubaki; S Kushiro; N Takasawa
Journal:  Acta Neuropathol       Date:  1978-04-26       Impact factor: 17.088

10.  Clinical heterogeneity in Korean patients with nemaline myopathy.

Authors:  Ji-Man Hong; Seung-Min Kim; Il-Nam Sunwoo; Se-Hoon Kim; Tai-Seung Kim; Dong-Suk Shim; Young-Chul Choi
Journal:  Yonsei Med J       Date:  2010-02-12       Impact factor: 2.759

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