Literature DB >> 12775505

Intranuclear rod myopathy, a rare and morphologically striking variant of nemaline rod myopathy.

Douglas A Weeks1, Randal R Nixon, Vassil Kaimaktchiev, Gary W Mierau.   

Abstract

A 4-year-old boy with muscle weakness underwent skeletal muscle biopsies. Light microscopy showed distinct eosinophilic inclusions within the majority of muscle cell nuclei, but none in the cytoplasm. Electron microscopy revealed crystalline, round to rod-shaped inclusions in the muscle cell nuclei. The inclusions stained positively for alpha-actinin. Intranuclear inclusions identical to those seen here have been described in rare cases of nemaline rod myopathy, though almost always together with classic intracytoplasmic rods. This case illustrates the importance of electron microscopy in the diagnosis of rare myopathies and in the characterization of cellular inclusions of unknown origin.

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Year:  2003        PMID: 12775505     DOI: 10.1080/01913120309933

Source DB:  PubMed          Journal:  Ultrastruct Pathol        ISSN: 0191-3123            Impact factor:   1.094


  4 in total

1.  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

2.  Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies.

Authors:  Clémence Labasse; Guy Brochier; Ana-Lia Taratuto; Bruno Cadot; John Rendu; Soledad Monges; Valérie Biancalana; Susana Quijano-Roy; Mai Thao Bui; Anaïs Chanut; Angéline Madelaine; Emmanuelle Lacène; Maud Beuvin; Helge Amthor; Laurent Servais; Yvan de Feraudy; Marcela Erro; Maria Saccoliti; Osorio Abath Neto; Julien Fauré; Béatrice Lannes; Vincent Laugel; Sandra Coppens; Fabiana Lubieniecki; Ana Buj Bello; Nigel Laing; Teresinha Evangelista; Jocelyn Laporte; Johann Böhm; Norma B Romero
Journal:  Acta Neuropathol Commun       Date:  2022-07-09       Impact factor: 7.578

Review 3.  Pathological defects in congenital myopathies.

Authors:  Caroline A Sewry
Journal:  J Muscle Res Cell Motil       Date:  2008-12-30       Impact factor: 2.698

4.  Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.

Authors:  Nozomu Yoshioka; Masayuki Kurose; Masato Yano; Dang Minh Tran; Shujiro Okuda; Yukiko Mori-Ochiai; Masao Horie; Toshihiro Nagai; Ichizo Nishino; Shinsuke Shibata; Hirohide Takebayashi
Journal:  Elife       Date:  2022-08-09       Impact factor: 8.713

  4 in total

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