Literature DB >> 29978728

Cerebral imaging in paediatric mitochondrial disorders.

Josef Finsterer1, Sinda Zarrouk-Mahjoub2.   

Abstract

OBJECTIVES: Because the central nervous system (CNS) is the second most frequently affected organ in mitochondrial disorders (MIDs) and since paediatric MIDs are increasingly recognised, it is important to know about the morphological CNS abnormalities on imaging in these patients. This review aims at summarising and discussing current knowledge and recent advances concerning CNS imaging abnormalities in paediatric MIDs.
METHODS: A systematic literature review was conducted.
RESULTS: The most relevant CNS abnormalities in paediatric MIDs on imaging include white and grey matter lesions, stroke-like lesions as the morphological equivalent of stroke-like episodes, cerebral atrophy, calcifications, optic atrophy, and lactacidosis. Because these CNS lesions may be seen with or without clinical manifestations, it is important to screen all MID patients for cerebral involvement. Some of these lesions may remain unchanged for years whereas others may be dynamic, either in the sense of progression or regression. Typical dynamic lesions are stroke-like lesions and grey matter lesions. Clinically relevant imaging techniques for visualisation of CNS abnormalities in paediatric MIDs are computed tomography, magnetic resonance (MR) imaging, MR spectroscopy, single-photon emission computed tomography, positron-emission tomography, and angiography.
CONCLUSIONS: CNS imaging in paediatric MIDs is important for diagnosing and monitoring CNS involvement. It also contributes to the understanding of the underlying pathomechanisms that lead to CNS involvement in MIDs.

Entities:  

Keywords:  Respiratory chain; brain; central nervous system; cerebrum; encephalomyopathy; mitochondrial; mitochondrion; multi-system disease; oxidative phosphorylation; spinal cord

Mesh:

Year:  2018        PMID: 29978728      PMCID: PMC6243461          DOI: 10.1177/1971400918786054

Source DB:  PubMed          Journal:  Neuroradiol J        ISSN: 1971-4009


  142 in total

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Authors:  Robert McFarland; Robert W Taylor; Douglass M Turnbull
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2.  Childhood-onset Leber hereditary optic neuropathy.

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3.  Japanese Leigh syndrome case treated with EPI-743.

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4.  [A case of stroke-like episode of MELAS of which progressive spread would be prevented by edaravone].

Authors:  Kengo Maeda; Mariko Tatsumi; Masayuki Tahara; Yoshiko Murata; Hiromichi Kawai; Hitoshi Yasuda
Journal:  Rinsho Shinkeigaku       Date:  2005-06

5.  Cerebral white matter involvement in children with mitochondrial encephalopathies.

Authors:  I Moroni; M Bugiani; A Bizzi; G Castelli; E Lamantea; G Uziel
Journal:  Neuropediatrics       Date:  2002-04       Impact factor: 1.947

6.  CT and MRI appearance of mitochondrial encephalopathy.

Authors:  K Geldof; K Ramboer; J M Goethals; L Verhaeghe
Journal:  JBR-BTR       Date:  2007 Jul-Aug

Review 7.  Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies.

Authors:  Maria Cristina Bianchi; Giuseppina Sgandurra; Michela Tosetti; Roberta Battini; Giovanni Cioni
Journal:  Biosci Rep       Date:  2007-06       Impact factor: 3.840

8.  [Case of Leber's hereditary optic neuropathy with mitochondrial DNA 11778 mutation exhibiting cerebellar ataxia, dilated cardiomyopathy and peripheral neuropathy].

Authors:  Yuka Watanabe; Masaaki Odaka; Koichi Hirata
Journal:  Brain Nerve       Date:  2009-03

9.  Novel insights into SLC25A46-related pathologies in a genetic mouse model.

Authors:  Maria Eirini Terzenidou; Aikaterini Segklia; Toshimi Kano; Florentia Papastefanaki; Alexandros Karakostas; Maria Charalambous; Fotis Ioakeimidis; Maria Papadaki; Ismini Kloukina; Margarita Chrysanthou-Piterou; Martina Samiotaki; George Panayotou; Rebecca Matsas; Eleni Douni
Journal:  PLoS Genet       Date:  2017-04-04       Impact factor: 5.917

10.  Transient neonatal renal failure and massive polyuria in MEGDEL syndrome.

Authors:  Carole Harbulot; Stéphanie Paquay; Imen Dorboz; Samia Pichard; Agnès Bourillon; Jean-François Benoist; Claude Jardel; Hélène Ogier de Baulny; Odile Boespflug-Tanguy; Manuel Schiff
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  2 in total

1.  Brain Atrophy and White Matter Damage Linked to Peripheral Bioenergetic Deficits in the Neurodegenerative Disease FXTAS.

Authors:  Junyi Wang; Eleonora Napoli; Kyoungmi Kim; Yingratana A McLennan; Randi J Hagerman; Cecilia Giulivi
Journal:  Int J Mol Sci       Date:  2021-08-25       Impact factor: 5.923

Review 2.  Mitochondrial Nucleic Acid as a Driver of Pathogenic Type I Interferon Induction in Mendelian Disease.

Authors:  Alice Lepelley; Timothy Wai; Yanick J Crow
Journal:  Front Immunol       Date:  2021-08-26       Impact factor: 7.561

  2 in total

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