Wikisage, the free encyclopedia of the second generation, is digital heritage
Doose syndrome: Difference between revisions
Jump to navigation
Jump to search
mNo edit summary |
mNo edit summary |
||
| Line 6: | Line 6: | ||
[http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2008.01765.x/full Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group] | [http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2008.01765.x/full Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group] | ||
<references/> | <references/> | ||
==ILAE== | |||
Version [[1989]] | |||
[[epilepsy with mioclonic atonic seizures]] | |||
Revision as of 00:40, 22 August 2017
Myoclonic astatic epilepsy was first described by Hermann Doose in 1970. It is an uncommon epilepsy that account 1-2% of all childhood epilepsies [1]
Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress