Synonyms: EPM1 | Progressive myoclonus epilepsy type 1 | ULD | Unverricht-Lundborg disease
A rare progressive myoclonic epilepsy (PME) disorder characterized by action- and stimulus-sensitive myoclonus and tonic-clonic seizures with ataxia but with only a mild cognitive decline over time.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version September 2024
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Progressive myoclonic epilepsy type 1?
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Advocacy Organizations
DDX3X Foundation
Our mission is to connect families, resources, and the medical community to advance research for a treatment or cure to DDX3X Syndrome. Our ultimate goal is to accelerate brain function in individuals affected by DDX3X Syndrome through advances in cell and gene therapy and pharmaceuticals.
Hope for ULD
Our mission is to improve the lives of those affected by Unverricht-Lundborg Disease by funding research, treatment, and education.
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Clinical Trials
For a list of clinical trials in this disease area, please click here.