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Ohtahara syndrome: Difference between revisions
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Ohtahara syndrome has its onset within in the first week of life. | [[Shunsuke Ohtahara|Ohtahara]] syndrome has its onset within in the first week of life. | ||
Supression burst is not only characteric of Ohtahara syndrome but also for [[Early mioclonus encephalopathy|EME]] (enhanced in sleep) | Supression burst is not only characteric of Ohtahara syndrome but also for [[Early mioclonus encephalopathy|EME]] (enhanced in sleep) | ||
[[Ketogenic diet]] has been shown efficient in EEE and other related syndrome as [[Dravet's syndrome|Dravet syndrome]]<ref>[http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2005.05705.x/epdf Ketogenic diet in patient with Dravet syndrome] Epilepsia 2005</ref> | [[Ketogenic diet]] has been shown efficient in EEE and other related syndrome as [[Dravet's syndrome|Dravet syndrome]]<ref>[http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2005.05705.x/epdf Ketogenic diet in patient with Dravet syndrome] Epilepsia 2005</ref> | ||
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[[Category:disease]] | [[Category:disease]] | ||
[[nl:Ohtahara syndrom]] | |||
Latest revision as of 17:53, 26 February 2016
Ohtahara syndrome has its onset within in the first week of life. Supression burst is not only characteric of Ohtahara syndrome but also for EME (enhanced in sleep) Ketogenic diet has been shown efficient in EEE and other related syndrome as Dravet syndrome[1] [2]
Links
Disease classification WHO
G40.3 Ohtahata syndrome
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