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Myoclonic Epilepsies, Progressive
A heterogeneous group of primarily familial EPILEPSY disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME.
Subtype terms (3)
More specific conditions that are subtypes of Myoclonic Epilepsies, Progressive in the MeSH hierarchy.
- Lafora Disease
2 drugs experimental
- MERRF Syndrome
- Unverricht-Lundborg Syndrome
3 drugs approved
Drugs by status
Phase 2 trials (1)
Phase 1 trials (1)
Organizations
Organization Involved with Phase 2 Indications (1)