Lafora disease

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Synonyms: EPM2 | PME type 2 | Progressive myoclonic epilepsy type 2 | Progressive myoclonus epilepsy type 2

A rare inherited severe progressive myoclonic epilepsy characterized by myoclonus and/or generalized seizures visual hallucinations (partial occipital seizures) and progressive neurological decline.

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 April 2026

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Lafora disease?

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Advocacy Organizations

Childhood Dementia Initiative

Our vision is for sustainable global health solutions for childhood dementia. This will be achieved through the following outcomes: - Treatments and cures available for children with dementia - Access to equitable and quality care for children with dementia and their families - Childhood dementia is a global health policy priority.

Pediatric Epilepsy Research Consortium

The Pediatric Epilepsy Research Consortium (PERC) is a group of US pediatric epilepsy centers, researchers and professionals in field of epilepsy whose goal is to provide a network and infrastructure to facilitate collegial, collaborative practice-changing research that will provide answers needed to improve the care of children with epilepsy.

website Location: National

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Clinical Trials

For a list of clinical trials in this disease area, please click here.