Lennox-Gastaut syndrome

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Lennox-Gastaut syndrome

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 March 2024

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Lennox-Gastaut syndrome?

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Advocacy Organizations

Rare Epilepsy Network (REN)

The mission of Rare Epilepsy Network (REN) is to work with urgency to collaboratively improve outcomes of rare epilepsy patients and families by fostering patient-focused research and advocacy.

Clinical Trials

For a list of clinical trials in this disease area, please click here.