Myoclonic Epilepsies, Progressive


Action Myoclonus Renal Failure Syndrome

Action Myoclonus-Renal Failure Syndrome

Ataxia, Chorea, Seizures, And Dementia

Atrophies, Dentatorubral-Pallidoluysian

Atrophy, Dentatorubral-Pallidoluysian

Atypical Inclusion Body Disease

Atypical Inclusion-Body Disease

Atypical Inclusion-Body Diseases

Biotin Responsive Encephalopathy

Biotin-Responsive Encephalopathies

Biotin-Responsive Encephalopathy

Dentatorubral Pallidoluysian Atrophy

Dentatorubral-Pallidoluysian Atrophies

Dentatorubral-Pallidoluysian Atrophy

Disease, Atypical Inclusion-Body

Disease, Naito-Oyanagi

Diseases, Atypical Inclusion-Body

Diseases, Naito-Oyanagi

Encephalopathies, Biotin-Responsive

Encephalopathy, Biotin-Responsive

Epilepsies, Progressive Myoclonic

Epilepsies, Progressive Myoclonus

Epilepsy, Progressive Myoclonic

Epilepsy, Progressive Myoclonus

Familial Progressive Myoclonic Epilepsy

Haw River Syndrome

Haw River Syndromes

Inclusion-Body Disease, Atypical

Inclusion-Body Diseases, Atypical

May White Syndrome

May-White Syndrome

Myoclonic Epilepsy, Progressive

Myoclonus Epilepsies, Progressive

Myoclonus Nephropathy Syndrome

Myoclonus-Nephropathy Syndrome

Myoclonus-Nephropathy Syndromes

Naito Oyanagi Disease

Naito-Oyanagi Disease

Naito-Oyanagi Diseases

Oyanagi Disease, Naito

Progressive Myoclonic Epilepsies

Progressive Myoclonic Epilepsy

Progressive Myoclonus Epilepsies

Progressive Myoclonus Epilepsy

River Syndrome, Haw

River Syndromes, Haw

Syndrome, Haw River

Syndrome, Myoclonus-Nephropathy

Syndromes, Haw River

Syndromes, Myoclonus-Nephropathy

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.