Other terms
Epilepsies, Progressive Myoclonic,Epilepsy, Progressive Myoclonic,Myoclonic Epilepsy, Progressive,Progressive Myoclonic Epilepsies,Progressive Myoclonic Epilepsy,Progressive Myoclonus Epilepsies,Epilepsies, Progressive Myoclonus,Epilepsy, Progressive Myoclonus,Myoclonus Epilepsies, Progressive,Myoclonus Epilepsy, Progressive,Progressive Myoclonus Epilepsy,Atypical Inclusion-Body Disease,Atypical Inclusion Body Disease,Atypical Inclusion-Body Diseases,Disease, Atypical Inclusion-Body,Diseases, Atypical Inclusion-Body,Inclusion-Body Disease, Atypical,Inclusion-Body Diseases, Atypical,May-White Syndrome,May White Syndrome,Dentatorubral-Pallidoluysian Atrophy,Atrophies, Dentatorubral-Pallidoluysian,Atrophy, Dentatorubral-Pallidoluysian,Dentatorubral Pallidoluysian Atrophy,Dentatorubral-Pallidoluysian Atrophies,Naito Oyanagi Disease,Oyanagi Disease, Naito,Familial Progressive Myoclonic Epilepsy,Action Myoclonus-Renal Failure Syndrome,Action Myoclonus Renal Failure Syndrome,Biotin-Responsive Encephalopathy,Biotin Responsive Encephalopathy,Biotin-Responsive Encephalopathies,Encephalopathies, Biotin-Responsive,Encephalopathy, Biotin-Responsive
Description
Myoclonic Epilepsies, Progressive: 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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