Literature DB >> 2092592

Involvement of respiratory muscles in cytoplasmic body myopathy--a pathology study.

E Bertini1, E Ricci, R Boldrini, S Servidei, S Fusilli, C Dionisi-Vici, C Bosman, E Bonilla.   

Abstract

A muscle biopsy and autopsy study of a child who died at 14 months of respiratory failure is described. A diagnosis of infantile cytoplasmic body myopathy was made due to the high percentage of cytoplasmic bodies (CBs), particularly in respiratory muscles. No pathological abnormalities were found in the central nervous system, peripheral nerves or visceral organs. Immunohistochemical studies suggested that the central core of CBs was stained for fibrillary actin, being surrounded by a positive signal for desmin. A differential diagnosis as to other conditions involving proliferation of CBs is discussed.

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Year:  1990        PMID: 2092592     DOI: 10.1016/s0387-7604(12)80010-6

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  6 in total

1.  Hereditary myopathy of the diaphragmatic muscles in Holstein-Friesian cattle.

Authors:  H Furuoka; T Doi; N Nakamura; I Inada; S Osame; T Matsui
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

2.  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

3.  Cytoplasmic body myopathy: familial cases with accumulation of desmin and dystrophin. An immunohistochemical, immunoelectron microscopic and biochemical study.

Authors:  A Caron; F Viader; B Lechevalier; F Chapon
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

4.  Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings.

Authors:  E Bertini; G Salviati; F Apollo; E Ricci; S Servidei; A Broccolini; M Papacci; P Tonali
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

5.  Titin mutation segregates with hereditary myopathy with early respiratory failure.

Authors:  Gerald Pfeffer; Hannah R Elliott; Helen Griffin; Rita Barresi; James Miller; Julie Marsh; Anni Evilä; Anna Vihola; Peter Hackman; Volker Straub; David J Dick; Rita Horvath; Mauro Santibanez-Koref; Bjarne Udd; Patrick F Chinnery
Journal:  Brain       Date:  2012-05-09       Impact factor: 13.501

6.  Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure.

Authors:  Gerald Pfeffer; Rita Barresi; Ian J Wilson; Steven A Hardy; Helen Griffin; Judith Hudson; Hannah R Elliott; Aravind V Ramesh; Aleksandar Radunovic; John B Winer; Sujit Vaidya; Ashok Raman; Mark Busby; Maria E Farrugia; Alec Ming; Chris Everett; Hedley C A Emsley; Rita Horvath; Volker Straub; Kate Bushby; Hanns Lochmüller; Patrick F Chinnery; Anna Sarkozy
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-03-13       Impact factor: 10.154

  6 in total

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