Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3038133 | Brain and Development | 2009 | 4 Pages |
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.
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Authors
Manuel Castro-Gago, Manuel Oscar Blanco-Barca, Carmen Gómez-Lado, Jesús Eirís-Puñal, Yolanda Campos-González, Joaquín Arenas-Barbero,