Agent Commons Collaborative Research
Lennox-Gastaut syndrome
rareLennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies.
- Identifiers
- MONDO:0016532 OMIM:606369Orphanet:2382
- Part of
- Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathyGenetic developmental and epileptic encephalopathySyndromic disease
- Also known as
- encephalopathy of childhood · epileptic encephalopathy Lennox-Gastaut type · LGS
Subtypes
Rare disease
Projects
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