Literature DB >> 17989367

Clinical and brain MR imaging features focusing on the brain stem and cerebellum in patients with myoclonic epilepsy with ragged-red fibers due to mitochondrial A8344G mutation.

S Ito1, W Shirai, M Asahina, T Hattori.   

Abstract

SUMMARY: We report 3 patients with myoclonic epilepsy with ragged-red fibers (MERRF) diagnosed by mitochondrial A8344G mutation. Cerebellar ataxia was the first symptom in all patients. Conventional brain MR imaging showed atrophy of the superior cerebellar peduncles and the cerebellum in all patients and brain stem atrophy in 2 patients. In diffusion tensor analysis, fractional anisotropy of the superior cerebellar peduncles was mildly decreased in 1 patient. There was a discrepancy between clinical disabilities (severe) and radiologic abnormalities (mild). This discrepancy and atrophy of the superior cerebellar peduncles and the cerebellum may be important findings suggesting a diagnosis of MERRF.

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Year:  2007        PMID: 17989367      PMCID: PMC8118999          DOI: 10.3174/ajnr.A0865

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  16 in total

1.  Apparent diffusion coefficient measurements of the middle cerebellar peduncle differentiate the Parkinson variant of MSA from Parkinson's disease and progressive supranuclear palsy.

Authors:  Giuseppe Nicoletti; Raffaele Lodi; Francesca Condino; Caterina Tonon; Francesco Fera; Emil Malucelli; David Manners; Mario Zappia; Letterio Morgante; Paolo Barone; Bruno Barbiroli; Aldo Quattrone
Journal:  Brain       Date:  2006-06-30       Impact factor: 13.501

2.  Effects of number of diffusion gradient directions on derived diffusion tensor imaging indices in human brain.

Authors:  H Ni; V Kavcic; T Zhu; S Ekholm; J Zhong
Journal:  AJNR Am J Neuroradiol       Date:  2006-09       Impact factor: 3.825

3.  Clinicopathological features of MERRF.

Authors:  N Fukuhara
Journal:  Muscle Nerve Suppl       Date:  1995

4.  Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.

Authors:  Chin-Chang Huang; Hung-Chou Kuo; Chen-Che Chu; Chia-Wei Liou; Yi-Shing Ma; Yau-Huei Wei
Journal:  J Biomed Sci       Date:  2002       Impact factor: 8.410

5.  The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.

Authors:  G M Fabrizi; E Cardaioli; G S Grieco; T Cavallaro; A Malandrini; L Manneschi; M T Dotti; A Federico; G Guazzi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-07       Impact factor: 10.154

6.  SPECT findings in mitochondrial encephalomyopathy.

Authors:  Y Watanabe; K Hashikawa; H Moriwaki; N Oku; Y Seike; R Kodaka; J Ono; T Uehara; H Kusuoka; T Nishimura
Journal:  J Nucl Med       Date:  1998-06       Impact factor: 10.057

7.  Neuropathology of myoclonus epilepsy associated with ragged-red fibers (Fukuhara's disease).

Authors:  S Takeda; K Wakabayashi; E Ohama; F Ikuta
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

8.  Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies.

Authors:  P M Mathews; F Andermann; K Silver; G Karpati; D L Arnold
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

9.  Analysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndrome.

Authors:  A Lombès; C Diaz; N B Romero; F Ziegler; M Fardeau
Journal:  Neuromuscul Disord       Date:  1992       Impact factor: 4.296

Review 10.  MERRF: a clinicopathological study. Relationships between myoclonus epilepsies and mitochondrial myopathies.

Authors:  N Fukuhara
Journal:  Rev Neurol (Paris)       Date:  1991       Impact factor: 2.607

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  13 in total

1.  Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutation.

Authors:  Florian Brackmann; Angela Abicht; Uwe Ahting; Rolf Schröder; Regina Trollmann
Journal:  Eur J Pediatr       Date:  2012-01-25       Impact factor: 3.183

Review 2.  Young-onset dementia.

Authors:  Dulanji K Kuruppu; Brandy R Matthews
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Review 3.  Mitochondrial DNA heteroplasmy in disease and targeted nuclease-based therapeutic approaches.

Authors:  Nadee Nissanka; Carlos T Moraes
Journal:  EMBO Rep       Date:  2020-02-19       Impact factor: 8.807

Review 4.  Posterior fossa involvement in the diagnosis of adult-onset inherited leukoencephalopathies.

Authors:  Xavier Ayrignac; Clemence Boutiere; Clarisse Carra-Dalliere; Pierre Labauge
Journal:  J Neurol       Date:  2016-04-28       Impact factor: 4.849

5.  Cerebellar atrophy is common among mitochondrial disorders.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Metab Brain Dis       Date:  2018-05-01       Impact factor: 3.584

Review 6.  Magnetic resonance imaging biomarkers in patients with progressive ataxia: current status and future direction.

Authors:  Stuart Currie; Marios Hadjivassiliou; Ian J Craven; Iain D Wilkinson; Paul D Griffiths; Nigel Hoggard
Journal:  Cerebellum       Date:  2013-04       Impact factor: 3.847

7.  Magnetic resonance imaging differential diagnosis of brainstem lesions in children.

Authors:  Carlo Cosimo Quattrocchi; Yuri Errante; Maria Camilla Rossi Espagnet; Stefania Galassi; Sabino Walter Della Sala; Bruno Bernardi; Giuseppe Fariello; Daniela Longo
Journal:  World J Radiol       Date:  2016-01-28

8.  "Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation.

Authors:  Michela Catteruccia; Donato Sauchelli; Giacomo Della Marca; Guido Primiano; Cristina Cuccagna; Daniela Bernardo; Milena Leo; Antonella Camporeale; Tommaso Sanna; Alessandro Cianfoni; Serenella Servidei
Journal:  J Neurol       Date:  2015-01-06       Impact factor: 4.849

Review 9.  The genetics of ataxia: through the labyrinth of the Minotaur, looking for Ariadne's thread.

Authors:  M Mancuso; D Orsucci; G Siciliano; U Bonuccelli
Journal:  J Neurol       Date:  2014-09       Impact factor: 4.849

Review 10.  Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.

Authors:  Sumit Parikh; Amy Goldstein; Mary Kay Koenig; Fernando Scaglia; Gregory M Enns; Russell Saneto; Irina Anselm; Bruce H Cohen; Marni J Falk; Carol Greene; Andrea L Gropman; Richard Haas; Michio Hirano; Phil Morgan; Katherine Sims; Mark Tarnopolsky; Johan L K Van Hove; Lynne Wolfe; Salvatore DiMauro
Journal:  Genet Med       Date:  2014-12-11       Impact factor: 8.822

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