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

Cure GABA-A Variants

Our vision at Cure GABA-A is a future where individuals living with GABA-A Variants experience improved quality of life and have access to personalized treatments. We envision a world where repurposed FDA-approved drugs and gene therapies offer hope and relief to patients, effectively managing symptoms and addressing the underlying genetic causes of GABA-A Variants. Our organization has the sole focus of understanding the most efficient and effective way to develop potential therapies for GABA-A Variants.

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.