Variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration
MONDO:0800495An epilepsy syndrome characterized by seizures along with developmental and/or epileptic encephalopathy or progressive neurological deterioration where age at seizure onset varies.
Also known as: VAE-SDE/PND
21 clinical trials for this condition and its sub-types, 0 tagged with Variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration itself.
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Browse by category →Sub-types of Variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration
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Progressive myoclonus epilepsy 5 trials · 12 incl. sub-types
15 sub-types
- MERRF syndrome 5 trials
- Lafora disease 1 trial Sub-types →
- Unverricht-Lundborg syndrome 1 trial
- Neuronal ceroid lipofuscinosis 8 northern epilepsy variant 1 trial
- Action myoclonus-renal failure syndrome 0 trials
- Early-onset Lafora body disease 0 trials
- Epilepsy, progressive myoclonic, 11 0 trials
- Epilepsy, progressive myoclonic, 12 0 trials
- Epilepsy, progressive myoclonic, 1B 0 trials
- Familial encephalopathy with neuroserpin inclusion bodies 0 trials
- Progressive myoclonic epilepsy type 3 0 trials
- Progressive myoclonic epilepsy type 6 0 trials
- Progressive myoclonic epilepsy type 7 0 trials
- Progressive myoclonic epilepsy type 8 0 trials
- Progressive myoclonic epilepsy type 9 0 trials
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Rasmussen subacute encephalitis 2 trials
Most studied deeper sub-types
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