| Descriptor English: | Myoclonic Epilepsies, Progressive | ||||||
| Descriptor Spanish: |
Epilepsias Mioclónicas Progresivas
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| Descriptor Portuguese: | Epilepsias Mioclônicas Progressivas | ||||||
| Descriptor French: | Épilepsies myocloniques progressives | ||||||
| Entry term(s): |
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 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 Progressive Myoclonic Epilepsies Progressive Myoclonic Epilepsy Progressive Myoclonus Epilepsies Progressive Myoclonus Epilepsy River Syndromes, Haw Syndromes, Myoclonus-Nephropathy |
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| Tree number(s): |
C10.228.140.490.375.130.650 C10.228.140.490.493.063.650 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020191 | ||||||
| Scope note: | 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Epilepsies, Myoclonic (1977-1999) Epilepsy (1965-1999) Myoclonus (1968-1999) |
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| Public MeSH Note: | 2000; see Epilepsy, Myoclonic 1977-1999 |
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| History Note: | 2000; use Epilepsy, Myoclonic 1977-1999 |
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| DeCS ID: | 34274 | ||||||
| Unique ID: | D020191 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/11/04 | ||||||
| Revision Date: | 2017/02/24 |
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Myoclonic Epilepsies, Progressive
- Preferred
Atypical Inclusion-Body Disease
- Narrower
May-White Syndrome
- Narrower
Dentatorubral-Pallidoluysian Atrophy
- Narrower
Familial Progressive Myoclonic Epilepsy
- Narrower
Action Myoclonus-Renal Failure Syndrome
- Narrower
Biotin-Responsive Encephalopathy
- Narrower
| Concept UI |
M0328687 |
| Scope note | 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. |
| Preferred term | Myoclonic Epilepsies, Progressive |
| Entry term(s) |
Epilepsies, Progressive Myoclonic Epilepsies, Progressive Myoclonus Epilepsy, Progressive Myoclonic Epilepsy, Progressive Myoclonus Myoclonic Epilepsy, Progressive Myoclonus Epilepsies, Progressive Progressive Myoclonic Epilepsies Progressive Myoclonic Epilepsy Progressive Myoclonus Epilepsies Progressive Myoclonus Epilepsy |
| Concept UI |
M0335759 |
| Preferred term | Atypical Inclusion-Body Disease |
| Entry term(s) |
Atypical Inclusion Body Disease Atypical Inclusion-Body Diseases Inclusion-Body Disease, Atypical Inclusion-Body Diseases, Atypical |
| Concept UI |
M0335758 |
| Preferred term | May-White Syndrome |
| Entry term(s) |
May White Syndrome |
| Concept UI |
M0335757 |
| Preferred term | Dentatorubral-Pallidoluysian Atrophy |
| Entry term(s) |
Ataxia, Chorea, Seizures, And Dementia Atrophies, Dentatorubral-Pallidoluysian Atrophy, Dentatorubral-Pallidoluysian Dentatorubral Pallidoluysian Atrophy Dentatorubral-Pallidoluysian Atrophies Haw River Syndrome Haw River Syndromes Naito Oyanagi Disease Naito-Oyanagi Disease Naito-Oyanagi Diseases River Syndromes, Haw |
| Concept UI |
M0335760 |
| Preferred term | Familial Progressive Myoclonic Epilepsy |
| Concept UI |
M0335755 |
| Preferred term | Action Myoclonus-Renal Failure Syndrome |
| Entry term(s) |
Action Myoclonus Renal Failure Syndrome Myoclonus Nephropathy Syndrome Myoclonus-Nephropathy Syndrome Myoclonus-Nephropathy Syndromes Syndromes, Myoclonus-Nephropathy |
| Concept UI |
M0335756 |
| Preferred term | Biotin-Responsive Encephalopathy |
| Entry term(s) |
Biotin Responsive Encephalopathy Biotin-Responsive Encephalopathies Encephalopathies, Biotin-Responsive Encephalopathy, Biotin-Responsive |
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