Genetic developmental and epileptic encephalopathy
MONDO:0100062A complex neurodevelopmental disorder characterized by a range of developmental delays and epileptic encephalopathy phenotypes. Seizure onset is variable and intellectual disability is variable in presence and severity.
Also known as: developmental and epileptic encephalopathy, hereditary developmental and epileptic encephalopathy
93 clinical trials for this condition and its sub-types, 2 tagged with Genetic developmental and epileptic encephalopathy itself.
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Sub-types of Genetic developmental and epileptic encephalopathy
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Dravet syndrome 39 trials
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Lennox-Gastaut syndrome 26 trials · 27 incl. sub-types
3 sub-types
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Neonatal-onset developmental and epileptic encephalopathy 0 trials · 5 incl. sub-types
20 sub-types
- Developmental and epileptic encephalopathy, 13 3 trials
- Developmental and epileptic encephalopathy, 25 1 trial
- Developmental and epileptic encephalopathy, 42 1 trial
- Developmental and epileptic encephalopathy, 12 0 trials
- Developmental and epileptic encephalopathy, 16 0 trials
- Developmental and epileptic encephalopathy, 21 0 trials
- Developmental and epileptic encephalopathy, 24 0 trials
- Developmental and epileptic encephalopathy, 26 0 trials
- Developmental and epileptic encephalopathy, 28 0 trials
- Developmental and epileptic encephalopathy, 29 0 trials
- Developmental and epileptic encephalopathy, 31A 0 trials
- Developmental and epileptic encephalopathy, 32 0 trials
- Developmental and epileptic encephalopathy, 33 0 trials
- Developmental and epileptic encephalopathy, 34 0 trials
- Developmental and epileptic encephalopathy, 39 0 trials
- Developmental and epileptic encephalopathy, 41 0 trials
- Developmental and epileptic encephalopathy, 44 0 trials
- Developmental and epileptic encephalopathy, 45 0 trials
- Developmental and epileptic encephalopathy, 46 0 trials
- Developmental and epileptic encephalopathy, 47 0 trials
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2 sub-types