Infantile epilepsy syndrome
MONDO:0020071An epilepsy syndrome that occurs between 28 days to one year of life.
Also known as: epilepsy syndrome of infancy, infantile epilepsy syndrome, infantile onset epilepsy syndrome
16 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Developmental and epileptic encephalopathy, 13
(3)
Intellectual disability, autosomal dominant 5
(2)
Developmental and epileptic encephalopathy, 25
(1)
Developmental and epileptic encephalopathy, 42
(1)
Undetermined early-onset epileptic encephalopathy
(1)
Benign familial infantile epilepsy
(0)
Benign familial neonatal-infantile seizures 1
(0)
Benign infantile focal epilepsy with midline spikes and wave during sleep
(0)
Benign infantile seizures associated with mild gastroenteritis
(0)
Benign non-familial infantile seizures
(0)
Benign partial epilepsy of infancy with complex partial seizures
(0)
Benign partial epilepsy with secondarily generalized seizures in infancy
(0)
Benign partial infantile seizures
(0)
Developmental and epileptic encephalopathy, 21
(0)
Developmental and epileptic encephalopathy, 24
(0)
Developmental and epileptic encephalopathy, 26
(0)
Developmental and epileptic encephalopathy, 28
(0)
Developmental and epileptic encephalopathy, 29
(0)
Developmental and epileptic encephalopathy, 31A
(0)
Developmental and epileptic encephalopathy, 32
(0)