Lennox Gastaut Syndrome

A childhood-onset epilepsy syndrome.

Year introduced: 2015

PubMed search builder options

Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C10.228.140.490.493.750, C16.320.495

MeSH Unique ID: D065768

Entry Terms:

• Lennox Gastaut Syndromes
• Lennox-Gastaut Syndrome

Previous Indexing:

• Spasms, Infantile (1988-2014)

All MeSH Categories
Diseases Category
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epileptic Syndromes
Lennox Gastaut Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Lennox Gastaut Syndrome