| Literature DB >> 18617342 |
Manuel Castro-Gago1, Manuel Oscar Blanco-Barca, Carmen Gómez-Lado, Jesús Eirís-Puñal, Yolanda Campos-González, Joaquín Arenas-Barbero.
Abstract
We report an infant with complex I deficiency of the mitochondrial respiratory chain whose most conspicuous symptom at presentation was an Ohtahara syndrome. Review of the literature suggest that association of these two conditions is extremely rare. Despite the few cases reported, in our view Ohtahara syndrome should be considered as one of the forms of presentation of mitochondrial dysfunction.Entities:
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Year: 2008 PMID: 18617342 DOI: 10.1016/j.braindev.2008.05.009
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961