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Progressive myoclonic epilepsy type 1
What is Progressive myoclonic epilepsy type 1?
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.
Other condition names
PME type 1
Progressive myoclonic epilepsy type 1
Progressive myoclonus epilepsy type 1
ULD
Inheritance type
Autosomal recessive
Age of Onset
Adolescent
Childhood
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.