SYNGAP1-related developmental and epileptic encephalopathy
Engelsk navn: SYNGAP1-related developmental and epileptic encephalopathy
Engelske synonym: SYNGAP1-related DEE
Definisjon
A rare genetic developmental and epileptic encephalopathy (DEE) characterized by developmental delay, generalized epilepsy consisting of eyelid myoclonia with absences and myoclonic-atonic seizures, intellectual disability and autism spectrum disorder (ASD).
Fra Orphanet
ORPHA: 544254
Klassifiseringsnivå: Disorder
ICD-10: G40.4