Wikisage, the free encyclopedia of the second generation, is digital heritage
Ohtahara syndrome: Difference between revisions
Jump to navigation
Jump to search
(DIMDI) |
(fix data) |
||
| Line 13: | Line 13: | ||
<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> | ||
*[[Landau–Kleffner syndrome]] | *[[Landau–Kleffner syndrome]] | ||
{{Wikidata| | {{Wikidata|Q649602}} | ||
<references/> | <references/> | ||
Revision as of 13:10, 7 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]
Links
Disease classification WHO
G40.3 Ohtahata syndrome
