Unverricht-Lundborg syndrome

Unverricht-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.

Also known as: PME type 1, ULD, Unverricht-Lundborg disease, Unverricht-Lundborg syndrome, epilepsy, progressive myoclonic 1A (Unverricht and Lundborg), progressive myoclonic epilepsy type 1, progressive myoclonus epilepsy type 1, Baltic myoclonic epilepsy

20 clinical trials for this condition and its sub-types, 1 tagged with Unverricht-Lundborg syndrome itself.