| D020191 |
Myoclonic Epilepsies, Progressive |
A heterogeneous group of primarily familial EPILEPSY 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. |
Action Myoclonus-Renal Failure Syndrome,Biotin-Responsive Encephalopathy,Dentatorubral-Pallidoluysian Atrophy,May-White Syndrome,Ataxia, Chorea, Seizures, And Dementia,Atypical Inclusion-Body Disease,Familial Progressive Myoclonic Epilepsy,Haw River Syndrome,Myoclonic Epilepsy, Progressive,Myoclonus-Nephropathy Syndrome,Naito Oyanagi Disease,Naito-Oyanagi Disease,Progressive Myoclonic Epilepsy,Progressive Myoclonus Epilepsies,Action Myoclonus Renal Failure Syndrome,Atrophies, Dentatorubral-Pallidoluysian,Atrophy, Dentatorubral-Pallidoluysian,Atypical Inclusion Body Disease,Atypical Inclusion-Body Diseases,Biotin Responsive Encephalopathy,Biotin-Responsive Encephalopathies,Dentatorubral Pallidoluysian Atrophy,Dentatorubral-Pallidoluysian Atrophies,Encephalopathies, Biotin-Responsive,Encephalopathy, Biotin-Responsive,Epilepsies, Progressive Myoclonic,Epilepsies, Progressive Myoclonus,Epilepsy, Progressive Myoclonic,Epilepsy, Progressive Myoclonus,Haw River Syndromes,Inclusion-Body Disease, Atypical,Inclusion-Body Diseases, Atypical,May White Syndrome,Myoclonus Epilepsies, Progressive,Myoclonus Nephropathy Syndrome,Myoclonus-Nephropathy Syndromes,Naito-Oyanagi Diseases,Progressive Myoclonic Epilepsies,Progressive Myoclonus Epilepsy,River Syndromes, Haw,Syndromes, Myoclonus-Nephropathy |
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