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Lennox–Gastaut syndrome: Difference between revisions
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{{disease|G40.4|Lennox-Gastaut syndrome}} | {{disease|G40.4|Lennox-Gastaut 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 | 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]] | [[nl:Syndroom van Lennox-Gastaut]] | ||
[[Category:Medicine]] | |||
Revision as of 04:15, 5 September 2015
Disease classification WHO
G40.4 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