Literature DB >> 8654494

Ragged red or ragged blue fibers.

H Reichmann1, L Vogler, P Seibel.   

Abstract

Fibers called ragged red fibers are generally considered the morphological characteristic of mitochondrial encephalomyopathies. These fibers appear red in the modified Gomori trichrome (Tri) stain due to subsarcolemmal and interfibrillar increase in mitochondrial number and volume. Other accepted morphological abnormalities include partial cytochrome c oxidase deficiency and subsarcolemmal increase in succinate dehydrogenase and NADH tetrazolium reductase stain. We were interested to see which of these abnormalities would be the most specific for mitochondrial cytopathies such as Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia. We analyzed five patients and found 74 fibers compatible with mitochondrial abnormalities as defined above. The modified Gomori Tri stain turned out to be the most specific and reliable technique.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8654494     DOI: 10.1159/000117217

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


  4 in total

Review 1.  Mitochondrial threshold effects.

Authors:  Rodrigue Rossignol; Benjamin Faustin; Christophe Rocher; Monique Malgat; Jean-Pierre Mazat; Thierry Letellier
Journal:  Biochem J       Date:  2003-03-15       Impact factor: 3.857

2.  Mice lacking TR4 nuclear receptor develop mitochondrial myopathy with deficiency in complex I.

Authors:  Su Liu; Yi-Fen Lee; Samuel Chou; Hideo Uno; Gonghui Li; Paul Brookes; Michael P Massett; Qiao Wu; Lu-Min Chen; Chawnshang Chang
Journal:  Mol Endocrinol       Date:  2011-05-26

3.  Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells.

Authors:  Selena Trifunov; Angela Pyle; Maria Lucia Valentino; Rocco Liguori; Patrick Yu-Wai-Man; Florence Burté; Jennifer Duff; Stephanie Kleinle; Isabel Diebold; Michela Rugolo; Rita Horvath; Valerio Carelli
Journal:  Sci Rep       Date:  2018-08-03       Impact factor: 4.379

4.  Camptocormia as a Novel Phenotype in a Heterozygous POLG2 Mutation.

Authors:  Diana Lehmann Urban; Leila Motlagh Scholle; Kerstin Alt; Albert C Ludolph; Angela Rosenbohm
Journal:  Diagnostics (Basel)       Date:  2020-01-26
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.