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A case of Ohtahara syndrome with cytochrome oxidase deficiency
A N Williams1, R G Gray, K Poulton
1Birmingham Children's Hospital, UK.
Developmental Medicine and Child Neurology
|September 24, 1998
Abstract:
Ohtahara syndrome is a rare cause of epileptic seizures during the neonatal period. This is believed to be the first report of this syndrome with a specific metabolic defect. Defects in respiratory chain function may be more common than previously assumed in patients with this epilepsy syndrome.