Myoclonic Epilepsies, Progressive |
| Atypical Inclusion-Body Disease; Familial Progressive Myoclonic Epilepsy; Progressive Myoclonic Epilepsy; Progressive Myoclonus Epilepsies; Action Myoclonus Renal Failure Syndrome; Atrophies, Dentatorubral-Pallidoluysian |
| 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. |
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