Lennox-Gastaut syndrome

Disease Export to PDF
Name:
Lennox-Gastaut syndrome
Description:
A rare, severe early-onset developmental epileptic encephalopathy characterized by the triad of intellectual impairment, multiple seizure types, and typical electroencephalography (EEG) abnormalities.
ORPHAcode:
2382
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14