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.
Year introduced: 2000
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Subheadings:
Tree Number(s): C10.228.140.490.375.130.650, C10.228.140.490.493.063.650
MeSH Unique ID: D020191
Entry Terms:
- Epilepsies, Progressive Myoclonic
- Epilepsy, Progressive Myoclonic
- Progressive Myoclonic Epilepsies
- Progressive Myoclonus Epilepsies
- Epilepsies, Progressive Myoclonus
- Epilepsy, Progressive Myoclonus
- Myoclonus Epilepsies, Progressive
- Progressive Myoclonus Epilepsy
- Progressive Myoclonic Epilepsy
- Myoclonic Epilepsy, Progressive
- Action Myoclonus-Renal Failure Syndrome
- Action Myoclonus Renal Failure Syndrome
- Myoclonus-Nephropathy Syndrome
- Myoclonus Nephropathy Syndrome
- Myoclonus-Nephropathy Syndromes
- Syndromes, Myoclonus-Nephropathy
- Biotin-Responsive Encephalopathy
- Biotin-Responsive Encephalopathies
- Biotin Responsive Encephalopathy
- Encephalopathies, Biotin-Responsive
- Encephalopathy, Biotin-Responsive
- Dentatorubral-Pallidoluysian Atrophy
- Atrophies, Dentatorubral-Pallidoluysian
- Atrophy, Dentatorubral-Pallidoluysian
- Dentatorubral-Pallidoluysian Atrophies
- Dentatorubral Pallidoluysian Atrophy
- Naito Oyanagi Disease
- Ataxia, Chorea, Seizures, And Dementia
- Haw River Syndrome
- Haw River Syndromes
- River Syndromes, Haw
- Naito-Oyanagi Disease
- Naito-Oyanagi Diseases
- May-White Syndrome
- May White Syndrome
- Atypical Inclusion-Body Disease
- Atypical Inclusion Body Disease
- Atypical Inclusion-Body Diseases
- Inclusion-Body Disease, Atypical
- Inclusion-Body Diseases, Atypical
- Familial Progressive Myoclonic Epilepsy
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