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
18 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
MERRF syndrome
(4)
Progressive myoclonus epilepsy
(4)
Rasmussen subacute encephalitis
(2)
Lafora disease
(1)
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant
(1)
Unverricht-Lundborg syndrome
(1)
Action myoclonus-renal failure syndrome
(0)
Early-onset Lafora body disease
(0)
Epilepsy, progressive myoclonic, 11
(0)
Epilepsy, progressive myoclonic, 12
(0)
Epilepsy, progressive myoclonic, 1B
(0)
Familial encephalopathy with neuroserpin inclusion bodies
(0)
Myoclonic epilepsy of Lafora 1
(0)
Myoclonic epilepsy of Lafora 2
(0)
Progressive myoclonic epilepsy type 3
(0)
Progressive myoclonic epilepsy type 6
(0)
Progressive myoclonic epilepsy type 7
(0)
Progressive myoclonic epilepsy type 8
(0)
Progressive myoclonic epilepsy type 9
(0)