Literature DB >> 1492653

Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome.

M Burgeois1, F Goutieres, D Chretien, P Rustin, A Munnich, J Aicardi.   

Abstract

We report 2 sisters with a degenerative neurological disorder presenting clinically as a leukodystrophy. CT scan and MRI demonstrated small symmetrical foci of necrosis in the substentia nigra and in the basal ganglia typical of Leigh syndrome and diffuse cerebral white matter abnormalities. In these patients a deficiency in complex II of the respiratory chain was demonstrated in isolated mitochondria from muscle, as well as in fibroblasts and lymphocytes.

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Year:  1992        PMID: 1492653     DOI: 10.1016/s0387-7604(12)80349-4

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  16 in total

Review 1.  Mitochondrial energy metabolism in neurodegeneration associated with methylmalonic acidemia.

Authors:  Daniela R Melo; Alicia J Kowaltowski; Moacir Wajner; Roger F Castilho
Journal:  J Bioenerg Biomembr       Date:  2011-02       Impact factor: 2.945

Review 2.  Mitochondrial encephalomyopathies: what next?

Authors:  S DiMauro
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 3.  Metabolic intermediates in lactic acidosis: compounds, samples and interpretation.

Authors:  F Poggi-Travert; D Martin; T Billette de Villemeur; J P Bonnefont; A Vassault; D Rabier; C Charpentier; P Kamoun; A Munnich; J M Saudubray
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 4.  Proton magnetic resonance spectroscopy in brain white matter disorders.

Authors:  N De Stefano; A Federico; D L Arnold
Journal:  Ital J Neurol Sci       Date:  1997-12

Review 5.  Alternative Fuels in Epilepsy and Amyotrophic Lateral Sclerosis.

Authors:  Tesfaye W Tefera; Kah Ni Tan; Tanya S McDonald; Karin Borges
Journal:  Neurochem Res       Date:  2016-11-21       Impact factor: 3.996

6.  Leigh syndrome: serial MR imaging and clinical follow-up.

Authors:  J Arii; Y Tanabe
Journal:  AJNR Am J Neuroradiol       Date:  2000-09       Impact factor: 3.825

7.  Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.

Authors:  T Bourgeron; D Chretien; J Poggi-Bach; S Doonan; D Rabier; P Letouzé; A Munnich; A Rötig; P Landrieu; P Rustin
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

Review 8.  Neuroimaging in mitochondrial disorders.

Authors:  Andrea L Gropman
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

Review 9.  Neuroimaging of mitochondrial disease.

Authors:  Russell P Saneto; Seth D Friedman; Dennis W W Shaw
Journal:  Mitochondrion       Date:  2008-05-23       Impact factor: 4.160

10.  Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiency.

Authors:  J P Harpey; D Heron; M Prudent; C Charpentier; P Rustin; G Ponsot; V Cormier-Daire
Journal:  J Inherit Metab Dis       Date:  1998-10       Impact factor: 4.982

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