SYNGAP1-related developmental and epileptic encephalopathy

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Name:
SYNGAP1-related developmental and epileptic encephalopathy
Description:
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).
ORPHAcode:
544254
Synonyms:
SYNGAP1-related DEE
XREF(s):
Analyte(s):
Created:
04 Feb 2020 - 15:13
Changed:
22 Jun 2023 - 16:14