Please sign in to follow a disease.
Epilepsy syndrome
MONDO:0015650A syndrome that has a characteristic cluster of clinical features and/or lectroencephalographic (EEG) findings that reflect underlying epileptic activity. It is often associated with a range of other health issues, including cognitive impairment, intellectual disability, physical gross motor and fine motor delays, speech and language deficits, and impacts to other bodily functions and may be supported by specific etiological findings—such as structural, genetic, metabolic, immune, or infectious causes or have an unknown etiology.
Also known as: epileptic syndrome, syndromic epilepsy
186 clinical trials for this condition and its sub-types, 2 tagged with Epilepsy syndrome itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Epilepsy syndrome
-
Childhood-onset epilepsy syndrome 18 trials · 106 incl. sub-types
16 sub-types
- Familial partial epilepsy 0 trials · 39 incl. sub-types Sub-types →
- Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy 0 trials · 37 incl. sub-types Sub-types →
- New-onset refractory status epilepticus 8 trials
- Childhood-onset idiopathic generalized epilepsy syndrome 0 trials · 7 incl. sub-types Sub-types →
- Childhood-onset self-limited focal epilepsy syndrome 0 trials · 3 incl. sub-types Sub-types →
- Atypical childhood epilepsy with centrotemporal spikes 1 trial
- Rolandic epilepsy-speech dyspraxia syndrome 0 trials · 1 incl. sub-types Sub-types →
- Landau-Kleffner syndrome 0 trials
- Sunflower syndrome 0 trials
- Acute encephalopathy with biphasic seizures and late reduced diffusion 0 trials
- Childhood-onset genetic generalized epilepsy syndrome 0 trials Sub-types →
- Cryptogenic late-onset epileptic spasms 0 trials
- Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation 0 trials
- Perioral myoclonia with absences 0 trials
- Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome 0 trials
- Self-limited childhood occipital epilepsy 0 trials Sub-types →
-
Neonatal/infantile epilepsy syndrome 1 trial · 55 incl. sub-types
3 sub-types
-
Variable age epilepsy syndrome 0 trials · 31 incl. sub-types
4 sub-types
- Variable-age onset idiopathic generalized epilepsy syndrome 0 trials · 17 incl. sub-types Sub-types →
- Variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration 0 trials · 14 incl. sub-types Sub-types →
- Variable-age onset combined generalized and focal epilepsy syndrome 0 trials Sub-types →
- Variable-age onset focal epilepsy syndrome 0 trials Sub-types →
-
Myoclonic epilepsy 1 trial · 16 incl. sub-types
7 sub-types
- Progressive myoclonus epilepsy 5 trials · 12 incl. sub-types Sub-types →
- Juvenile myoclonic epilepsy 3 trials Sub-types →
- Epilepsy, familial adult myoclonic 0 trials Sub-types →
- Familial infantile myoclonic epilepsy 0 trials
- Myoclonic epilepsy in infancy 0 trials
- Myoclonic epilepsy in non-progressive encephalopathies 0 trials
- Myoclonic epilepsy, Hartung type 0 trials
-
Infantile epilepsy syndrome 2 trials · 10 incl. sub-types
9 sub-types
- Undetermined early-onset epileptic encephalopathy 1 trial · 6 incl. sub-types Sub-types →
- Intellectual disability, autosomal dominant 5 2 trials
- Benign partial infantile seizures 0 trials Sub-types →
- Idiopathic hemiconvulsion-hemiplegia syndrome 0 trials
- Infant epilepsy with migrant focal crisis 0 trials
- Infantile spasms-broad thumbs syndrome 0 trials
- Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression 0 trials
- Myoclonic epilepsy in infancy 0 trials
- Progressive myoclonic epilepsy with dystonia 0 trials
-
Neonatal epilepsy syndrome 1 trial · 7 incl. sub-types
6 sub-types
- Undetermined early-onset epileptic encephalopathy 1 trial · 6 incl. sub-types Sub-types →
- Benign idiopathic neonatal seizures 0 trials
- Benign neonatal seizures 0 trials Sub-types →
- Developmental and epileptic encephalopathy, 39 0 trials
- Malignant migrating partial seizures of infancy 0 trials Sub-types →
- Severe neonatal-onset encephalopathy with microcephaly 0 trials
-
Benign focal seizures of adolescence 0 trials