Lennox-Gastaut Syndrome (LGS)

Alias:
Lennox Syndrome
Lennox Gastaut Syndrome
Lgs
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Lennox-Gastaut Syndrome, also known as lennox syndrome, is related to west syndrome and epilepsy, and has symptoms including hemiplegia An important gene associated with Lennox-Gastaut Syndrome is CHD2 (Chromodomain Helicase DNA Binding Protein 2), and among its related pathways/superpathways are Transmission across Chemical Synapses and Sweet Taste Signaling. The drugs Liver Extracts and Rufinamide have been mentioned in the context of this disorder. Affiliated tissues include brain and eye, and related phenotypes are intellectual disability and encephalopathy
Related ID:
MESH:D065768
ICD11:651135242

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Infant
1-9/1000000
70
786
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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