Literature DB >> 15885549

[Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene].

S Monnot1, B Chabrol, A Cano, J F Pellissier, P Collignon, M F Montfort, V Paquis-Flucklinger.   

Abstract

Leigh syndrome is a heterogeneous disorder, usually due to a defect in oxidative metabolism. Mutations in SURF1 gene have been identified in patients with cytochrome c oxidase deficiency. We report a homozygous splice site deletion [516-2_516-1delAG] in a young girl presenting with cytochrome c oxidase-deficient Leigh syndrome. Identification of molecular defect is indispensable for genetic counselling and prenatal diagnosis.

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Year:  2005        PMID: 15885549     DOI: 10.1016/j.arcped.2005.01.019

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  2 in total

Review 1.  Cardiological manifestations of mitochondrial respiratory chain disorders.

Authors:  A Berardo; O Musumeci; A Toscano
Journal:  Acta Myol       Date:  2011-06

2.  Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease.

Authors:  M Pronicki; E Matyja; D Piekutowska-Abramczuk; T Szymanska-Debinska; A Karkucinska-Wieckowska; E Karczmarewicz; W Grajkowska; T Kmiec; E Popowska; J Sykut-Cegielska
Journal:  J Clin Pathol       Date:  2007-10-01       Impact factor: 3.411

  2 in total

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