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Lennox–Gastaut syndrome: Difference between revisions

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{{disease|G40.4|Lennox-Gastaut syndrome}}
#redirect [[Lennox-Gastaut syndrome]]
The L.-G syndrome is a difficult-to-treat form of childhood-onset [[epilepsy]] that most often appears between the second and sixth year of life, and is characterized by frequent seizures and different seizure types; it is often accompanied by developmental delay and psychological and behavioral problems
[[nl:Syndroom van Lennox-Gastaut]]
[[Category:Medicine]]

Latest revision as of 22:31, 31 January 2016

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