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Article

Lennox-Gastaut syndrome of unknown cause: phenotypic characteristics of patients in the Epilepsy Phenome/Genome Project.

Epilepsia - 1 Nov 2013

Widdess-Walsh Peter, Dlugos Dennis, Fahlstrom Robyn, Joshi Sucheta, Shellhaas Renée, Boro Alex, Sullivan Joseph, Geller Eric

Abstract excerpt

PURPOSE: Lennox-Gastaut syndrome (LGS) is a devastating childhood-onset epilepsy syndrome. The cause is unknown in 25% of cases. Little has been described about the specific clinical or electroencephalography (EEG) features of LGS of unknown or genetic cause (LGS(u)). The Epilepsy Phenome/Genome Project (EPGP) aims to characterize LGS(u) by phenotypic analysis of patients with LGS(u) and their parents. METHODS:...

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Identifiers

PMID: 24116958
DOI: 10.1111/epi.12395

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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