Background. A 20-year-old woman presented to a specialist epilepsy center with a 3-year history of drug-resistant epileptic seizures, progressive myoclonus, ataxia, and cognitive decline.
The 45-year-old patient has suffered from genetically confirmed progressive myoclonic epilepsy since the age of 8 years. The clinical picture was long dominated by action myoclonus, drop seizures ...
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