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.
推出的年份: 2000
树号: C10.228.140.490.375.130.650, C10.228.140.490.493.063.650
MeSH 单一 ID: D020191
进入的组:
Epilepsies, Progressive Myoclonic
Epilepsy, Progressive Myoclonic
Progressive Myoclonic Epilepsies
Progressive Myoclonic Epilepsy
Myoclonic Epilepsy, Progressive
Progressive Myoclonus Epilepsies
Epilepsies, Progressive Myoclonus
Epilepsy, Progressive Myoclonus
Myoclonus Epilepsies, Progressive
Progressive Myoclonus Epilepsy
Atypical Inclusion-Body Disease
Atypical Inclusion Body Disease
Atypical Inclusion-Body Diseases
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
Naito-Oyanagi Diseases
Haw River Syndrome
Haw River Syndromes
River Syndromes, Haw
Naito Oyanagi Disease
Ataxia, Chorea, Seizures, And Dementia
Familial Progressive Myoclonic Epilepsy
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 Encephalopathy
Biotin-Responsive Encephalopathies
Encephalopathies, Biotin-Responsive
Encephalopathy, Biotin-Responsive
早前的内容:
Epilepsies, Myoclonic (1977-1999)
Epilepsy (1965-1999)
Myoclonus (1968-1999)
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