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Progressive Myoclonic Epilepsy
| Name: | Progressive Myoclonic Epilepsy |
| Definition: | 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). |
| Super-category: | Myoclonic Epilepsy |
| Id: | birnlex_12722 |
| Link to OWL / RDF: | Download this content as OWL/RDF |
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Subcategories
This category has the following 3 subcategories, out of 3 total.
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U
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| 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 + |
| ModifiedDate | 29 May 2009 + |