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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. | Ohtahara syndrome has its onset within in the first week of life. | ||
[[Ketogenic diet]] has been shown efficient in EEE and other syndrome as [[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> | ||
==Links== | ==Links== | ||
[[Supression burst]] | [[Supression burst]] | ||
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<ref>[http://www.ncbi.nlm.nih.gov/static/header_footer_ajax/submenu/#howto Substantial and sustained seizure reduction with ketogenic diet in a patient with Ohtahara syndrome]</ref> | <ref>[http://www.ncbi.nlm.nih.gov/static/header_footer_ajax/submenu/#howto Substantial and sustained seizure reduction with ketogenic diet in a patient with Ohtahara syndrome]</ref> | ||
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Revision as of 11:43, 7 February 2016
Ohtahara syndrome has its onset within in the first week of life.
Ketogenic diet has been shown efficient in EEE and other related syndrome as Dravet syndrome[1]
