Literature DB >> 19344965

CMR gives clue to "ragged red fibers" in the heart in a patient with mitochondrial myopathy.

Tania Jose, Hans-Jürgen Gdynia, Heiko Mahrholdt, Matthias Vöhringer, Karin Klingel, Reinhard Kandolf, Antje Bornemann, Ali Yilmaz.   

Abstract

Mitochondrial myopathy may manifest either as isolated myopathy or as a neuromuscular multisystemic disease and is caused by genetic defects in the mitochondrial genome resulting in respiratory chain disorders. MELAS, which is characterised by mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes due to gene mutations in the mitochondrial DNA (adenine-to-guanine transition at nucleotide pair 3243, m.3243A>G), constitutes such a mitochondrial multisystemic disease. Although hypertrophied or dilated cardiomyopathy is quite common in MELAS, there have been no cardiovascular magnetic resonance (CMR)-based studies in these patients so far. This case report represents the first case in which comprehensive CMR and endomyocardial biopsy (EMB) data were obtained in the same patient with mitochondrial myopathy. Late gadolinium enhancement (LGE) imaging demonstrated a unique pattern of myocardial damage and histological work-up revealed the presence of "ragged red fibers" (conglomerates of mitochondria) in the heart tissue verifying the diagnosis of a mitochondrial cardiomyopathy as part of the underlying mitochondrial disease MELAS.
Copyright © 2009 Elsevier Ireland Ltd. All rights reserved.

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Year:  2009        PMID: 19344965     DOI: 10.1016/j.ijcard.2009.03.057

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  6 in total

1.  Cardiovascular magnetic resonance imaging (CMR) reveals characteristic pattern of myocardial damage in patients with mitochondrial myopathy.

Authors:  Ali Yilmaz; Hans-Jürgen Gdynia; Matthias Ponfick; Sabine Rösch; Alfred Lindner; Albert C Ludolph; Udo Sechtem
Journal:  Clin Res Cardiol       Date:  2011-12-06       Impact factor: 5.460

Review 2.  The genetics of dilated cardiomyopathy.

Authors:  Lisa Dellefave; Elizabeth M McNally
Journal:  Curr Opin Cardiol       Date:  2010-05       Impact factor: 2.161

Review 3.  Diagnosis and treatment of mitochondrial myopathies.

Authors:  Gerald Pfeffer; Patrick F Chinnery
Journal:  Ann Med       Date:  2011-08-25       Impact factor: 4.709

4.  Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy.

Authors:  Anca Florian; Anna Ludwig; Bianca Stubbe-Dräger; Matthias Boentert; Peter Young; Johannes Waltenberger; Sabine Rösch; Udo Sechtem; Ali Yilmaz
Journal:  J Cardiovasc Magn Reson       Date:  2015-05-22       Impact factor: 5.364

5.  Phenotypic Heterogeneity in 5 Family Members with the Mitochondrial Variant m.3243A>G.

Authors:  Josef Finsterer; Franco Laccone
Journal:  Am J Case Rep       Date:  2020-11-25

6.  Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.

Authors:  Hannah Kennedy; Tobias B Haack; Verity Hartill; Lavinija Mataković; E Regula Baumgartner; Howard Potter; Richard Mackay; Charlotte L Alston; Siobhan O'Sullivan; Robert McFarland; Grainne Connolly; Caroline Gannon; Richard King; Scott Mead; Ian Crozier; Wandy Chan; Chris M Florkowski; Martin Sage; Thomas Höfken; Bader Alhaddad; Laura S Kremer; Robert Kopajtich; René G Feichtinger; Wolfgang Sperl; Richard J Rodenburg; Jean Claude Minet; Angus Dobbie; Tim M Strom; Thomas Meitinger; Peter M George; Colin A Johnson; Robert W Taylor; Holger Prokisch; Kit Doudney; Johannes A Mayr
Journal:  Am J Hum Genet       Date:  2016-08-11       Impact factor: 11.025

  6 in total

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