Neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy

MONDO:0800490

A neonatal/infantile epilepsy syndrome characterized by the onset of non-self-limiting seizures and developmental regression or delay in infants/neonates. This condition is typically caused by genetic mutations that disrupt normal brain development, affecting both cognitive and motor development that is not responsive to typical seizure treatments.

Also known as: NIE-SDE

62 clinical trials for this condition and its sub-types, 0 tagged with Neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy itself.

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↑ Neonatal/infantile epilepsy syndrome (55)

Sub-types of Neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy

Dravet syndrome 39 trials
Infantile spasms 8 trials · 19 incl. sub-types
8 sub-types
- Developmental and epileptic encephalopathy, 2 10 trials
- Developmental and epileptic encephalopathy, 1 2 trials
- Developmental and epileptic encephalopathy, 12 0 trials
- Developmental and epileptic encephalopathy, 15 0 trials
- Developmental and epileptic encephalopathy, 27 0 trials
- Developmental and epileptic encephalopathy, 30 0 trials
- Developmental and epileptic encephalopathy, 40 0 trials
- Developmental and epileptic encephalopathy, 5 0 trials
Early-infantile DEE 2 trials
3 sub-types
- Developmental and epileptic encephalopathy, 3 0 trials
- Developmental and epileptic encephalopathy, 30 0 trials
- Developmental and epileptic encephalopathy, 41 0 trials
Epilepsy of infancy with migrating focal seizures 1 trial

Including sub-types (62) Tagged with Neonatal/infantile-onset epilepsy syndrome with developmental and epileptic encephalopathy (0)

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