| Literature DB >> 15885549 |
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.Entities:
Mesh:
Substances:
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