Literature DB >> 7676812

Desmin myopathy with cardiomyopathy.

C H Cameron1, M Mirakhur, I V Allen.   

Abstract

We report a case of abnormal desmin accumulation within the muscle of a 30-year-old female with a 2-year history of cardiomyopathy and axial muscle weakness. Serum creatine kinase was normal. A quadriceps muscle biopsy revealed pink hyaline inclusions, which stained for acid phosphatase and with PAS and were present in both fibre types. Electron microscopy showed these inclusions to consist of aggregates of irregularly arranged 6- to 15-nm-diameter filaments enmeshed within a central core of dense granulo-amorphous material. In other areas, the granulo-amorphous material lay as irregular patches within the sarcoplasm, mainly at the level of the "Z" band causing disruption of the sarcomere. Immunoelectron microscopy using colloidal gold showed that the dense amorphous material reacted strongly with desmin antisera and could, therefore, represent a defective or phosphorylated form of the protein.

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Year:  1995        PMID: 7676812     DOI: 10.1007/bf00571512

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  23 in total

1.  Axonal filamentous spheroids associated with cardiomyopathy with "targetoid fibers". I. Clinical, histologic, and electron microscopic studies.

Authors:  H M Liu; M Gumbinas
Journal:  Neurology       Date:  1974-06       Impact factor: 9.910

2.  Skeletal muscle in idiopathic cardiomyopathy.

Authors:  S A Shafig; M A Sande; R R Carruthers; T Killip; A T Milhorat
Journal:  J Neurol Sci       Date:  1972-03       Impact factor: 3.181

3.  [A new familial muscular disorder demonstrated by the intra-sarcoplasmic accumulation of a granulo-filamentous material which is dense on electron microscopy (author's transl)].

Authors:  M Fardeau; J Godet-Guillain; F M Tome; H Collin; S Gaudeau; C Boffety; P Vernant
Journal:  Rev Neurol (Paris)       Date:  1978 Jun-Jul       Impact factor: 2.607

4.  An unusual familial cardiomyopathy characterized by aberrant accumulations of desmin-type intermediate filaments.

Authors:  M E Stoeckel; M Osborn; A Porte; A Sacrez; A Batzenschlager; K Weber
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1981

5.  Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study.

Authors:  E Bertini; C Bosman; E Ricci; S Servidei; R Boldrini; M Sabatelli; G Salviati
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

6.  Myopathy associated with desmin type intermediate filaments. An immunoelectron microscopic study.

Authors:  J F Pellissier; J Pouget; C Charpin; D Figarella
Journal:  J Neurol Sci       Date:  1989-01       Impact factor: 3.181

7.  Subsarcolemmal vermiform deposits in skeletal muscle, associated with familial cardiomyopathy: report of two cases of a new entity.

Authors:  A Calderon; L E Becker; E G Murphy
Journal:  Pediatr Neurosci       Date:  1987

8.  Intermediate filament reconstitution in vitro. The role of phosphorylation on the assembly-disassembly of desmin.

Authors:  M Inagaki; Y Gonda; M Matsuyama; K Nishizawa; Y Nishi; C Sato
Journal:  J Biol Chem       Date:  1988-04-25       Impact factor: 5.157

9.  A form of congenital muscular dystrophy.

Authors:  H H Goebel; H G Lenard; U Langenbeck; B Mehl
Journal:  Brain Dev       Date:  1980       Impact factor: 1.961

Review 10.  Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle.

Authors:  M Sabatelli; E Bertini; E Ricci; G Salviati; S Magi; M Papacci; P Tonali
Journal:  J Neurol Sci       Date:  1992-05       Impact factor: 3.181

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  1 in total

1.  Dystrophin and the cardiomyocyte membrane cytoskeleton in the healthy and failing heart.

Authors:  R R Kaprielian; N J Severs
Journal:  Heart Fail Rev       Date:  2000-10       Impact factor: 4.214

  1 in total

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