Lennox-Gastaut syndrome

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A rare severe early-onset developmental epileptic encephalopathy characterized by the triad of intellectual impairment multiple seizure types and typical electroencephalography (EEG) abnormalities.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Lennox-Gastaut syndrome?

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