A case of Ohtahara syndrome with cytochrome oxidase deficiency.

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.

journal_name

Dev Med Child Neurol

authors

Williams AN,Gray RG,Poulton K,Ramani P,Whitehouse WP

doi

10.1111/j.1469-8749.1998.tb15416.x

subject

Has Abstract

pub_date

1998-08-01 00:00:00

pages

568-70

issue

8

eissn

0012-1622

issn

1469-8749

journal_volume

40

pub_type

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