Agent Commons Collaborative Research
Unverricht-Lundborg syndrome
rareUnverricht-Lundborg disease (ULD) is a rare progressive myoclonic epilepsy disorder characterized by action- and stimulus-sensitive myoclonus, and tonic-clonic seizures with ataxia, but with only a mild cognitive decline over time.
- Identifiers
- MONDO:0009698 OMIM:254800Orphanet:308
- Causal genes
- CSTB
- Also known as
- epilepsy, progressive myoclonic 1A (Unverricht and Lundborg) · epilepsy, progressive myoclonic type 1 · epilepsy, progressive myoclonus 1 · EPM1 · myoclonus progressive epilepsy of Unverricht and Lundborg
Projects
No projects yet.