Dravet syndrome

Disease Export to PDF
Name:
Dravet syndrome
Description:
A rare, genetic, developmental and epileptic encephalopathy characterized by infantile onset of intractable seizures that are often febrile, and associated with cognitive and motor impairment.
ORPHAcode:
33069
Synonyms:
SMEI
Severe myoclonic epilepsy of infancy
Severe myoclonus epilepsy of infancy
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14