Literature DB >> 17200493

Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.

Rita Horvath1, Rudolf Andre Kley, Hanns Lochmüller, Matthias Vorgerd.   

Abstract

We describe a patient who presented with parkinsonism associated with the A8344G myoclonus epilepsy, ataxia, and myopathy with ragged red fibers mutation in the tRNA(Lys) gene. In addition, neurogenic changes and mitochondrial myopathy with ragged red fibers were observed. Neither myoclonus epilepsy nor other clinical signs described in association with A8344G were noted. Similar to previously reported patients with parkinsonism and mtDNA deletions, the symptoms of our patient responded favorably to levodopa therapy.

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Year:  2007        PMID: 17200493     DOI: 10.1212/01.wnl.0000250334.48038.7a

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  17 in total

1.  A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes.

Authors:  Ioannis Zaganas; Helen Latsoudis; Eufrosini Papadaki; Pelagia Vorgia; Martha Spilioti; Andreas Plaitakis
Journal:  J Neurol       Date:  2009-02-27       Impact factor: 4.849

2.  Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.

Authors:  David K Simon; Nathan Pankratz; Diane K Kissell; Michael W Pauciulo; Cheryl A Halter; Alice Rudolph; Ronald F Pfeiffer; William C Nichols; Tatiana Foroud
Journal:  BMC Med Genet       Date:  2010-04-01       Impact factor: 2.103

Review 3.  Movement disorders in mitochondrial disease.

Authors:  Roula Ghaoui; Carolyn M Sue
Journal:  J Neurol       Date:  2018-01-06       Impact factor: 4.849

Review 4.  The role of mitochondria in neurodegenerative diseases.

Authors:  Massimiliano Filosto; Mauro Scarpelli; Maria Sofia Cotelli; Valentina Vielmi; Alice Todeschini; Valeria Gregorelli; Paola Tonin; Giuliano Tomelleri; Alessandro Padovani
Journal:  J Neurol       Date:  2011-05-22       Impact factor: 4.849

Review 5.  Mitochondrial DNA damage and repair in neurodegenerative disorders.

Authors:  Jenq-Lin Yang; Lior Weissman; Vilhelm A Bohr; Mark P Mattson
Journal:  DNA Repair (Amst)       Date:  2008-05-07

Review 6.  How can we treat mitochondrial encephalomyopathies? Approaches to therapy.

Authors:  Rita Horvath; Grainne Gorman; Patrick F Chinnery
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

Review 7.  POLG1-related and other "mitochondrial Parkinsonisms": an overview.

Authors:  Daniele Orsucci; Elena Caldarazzo Ienco; Michelangelo Mancuso; Gabriele Siciliano
Journal:  J Mol Neurosci       Date:  2011-01-08       Impact factor: 3.444

Review 8.  Tissue-specific implications of mitochondrial alterations in aging.

Authors:  Danhui Liu; Hongzhi Li; Jianxin Lu; Yidong Bai
Journal:  Front Biosci (Elite Ed)       Date:  2013-01-01

Review 9.  Mitochondrial DNA sequence variation and neurodegeneration.

Authors:  Michelangelo Mancuso; Massimiliano Filosto; Daniele Orsucci; Gabriele Siciliano
Journal:  Hum Genomics       Date:  2008-09       Impact factor: 4.639

Review 10.  Movement disorders and inborn errors of metabolism in adults: a diagnostic approach.

Authors:  F Sedel; J-M Saudubray; E Roze; Y Agid; M Vidailhet
Journal:  J Inherit Metab Dis       Date:  2008-05-30       Impact factor: 4.750

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