par Zupanc, Mary M.L.;Legros, Benjamin 
Référence Cerebellum, 3, 3, page (156-171)
Publication Publié, 2004-12
Référence Cerebellum, 3, 3, page (156-171)
Publication Publié, 2004-12
Article révisé par les pairs
| Résumé : | Progressive myoclonic epilepsies (PMEs) are a group of rare disorders characterized by the occurrence of seizures, myoclonus, and progressive neurological dysfunction. This article discusses epidemiology, genetics, pathology, clinical manifestations, EEG characteristics, methods of diagnosis and treatment of the most common causes of PME, including Unverricht-Lundborg Disease (Baltic Myoclonus), MERRF, neuronal ceroid lipofuscinosis, dentatorubropallidoluysan atrophy, Gaucher disease, Lafora disease, and sialidosis. The aim of this paper is to provide clinicians with useful clinical information in order to facilitate the diagnosis and treatment of these rare diseases. |
