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From NeuroLex
| Category:Progressive Myoclonic Epilepsy |
| Created | 8 October 2007 + |
|---|---|
| CurationStatus | uncurated + |
| Definition | A heterogeneous group of primarily familia … A heterogeneous group of primarily familial disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME (MeSH). , and UNVERRICHT-LUNDBORG SYNDROME (MeSH). |
| DefinitionSource | MeSH + |
| Id | birnlex_12722 + |
| Label | Progressive Myoclonic Epilepsy + |
| Modification dateThis property is a special property in this wiki. | 29 May 2009 21:53:08 + |
| ModifiedDate | 29 May 2009 + |
| Categories | Myoclonic Epilepsy |
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