| Descriptor English: | Epilepsy, Rolandic | ||||||
| Descriptor Spanish: |
Epilepsia Rolándica
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| Descriptor Portuguese: | Epilepsia Rolândica | ||||||
| Descriptor French: | Épilepsie rolandique | ||||||
| Entry term(s): |
BCECTS BECTS Benign Childhood Epilepsy With Centro Temporal Spikes Benign Childhood Epilepsy With Centro-Temporal Spikes Benign Epilepsy Of Childhood With Centrotemporal Spikes Benign Epilepsy With Centrotemporal Spikes Benign Rolandic Epilepsy Benign Rolandic Epilepsy of Childhood Centralopathic Epilepsies Centralopathic Epilepsy Centrotemporal Epilepsies Centrotemporal Epilepsy Epilepsies, Centralopathic Epilepsies, Centrotemporal Epilepsies, Rolandic Epilepsies, Temporal-Central Focal Epilepsy, Benign Rolandic Epilepsy, Centralopathic Epilepsy, Centrotemporal Epilepsy, Rolands Epilepsy, Sylvian Epilepsy, Temporal-Central Focal Focal Epilepsies, Temporal-Central Focal Epilepsy, Temporal-Central Rolandic Epilepsies Rolandic Epilepsy Rolandic Epilepsy, Benign Rolands Epilepsy Sylvian Epilepsy Temporal Central Focal Epilepsy Temporal-Central Focal Epilepsies Temporal-Central Focal Epilepsy |
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| Tree number(s): |
C10.228.140.490.360.280 C10.228.140.490.493.250 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D019305 | ||||||
| Scope note: | An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41) |
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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: |
Epilepsy, Partial (1986-1996) |
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| Public MeSH Note: | 1997 |
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| History Note: | 1997 |
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| DeCS ID: | 32946 | ||||||
| Unique ID: | D019305 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1997/01/01 | ||||||
| Date of Entry: | 1996/06/13 | ||||||
| Revision Date: | 2017/02/24 |
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Epilepsy, Rolandic
- Preferred
Benign Rolandic Epilepsy
- Narrower
| Concept UI |
M0028742 |
| Scope note | An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41) |
| Preferred term | Epilepsy, Rolandic |
| Entry term(s) |
Epilepsies, Rolandic Epilepsy, Rolands Epilepsy, Sylvian Rolandic Epilepsies Rolandic Epilepsy Rolands Epilepsy Sylvian Epilepsy |
| Concept UI |
M0521137 |
| Preferred term | Benign Rolandic Epilepsy |
| Entry term(s) |
BCECTS BECTS Benign Childhood Epilepsy With Centro Temporal Spikes Benign Childhood Epilepsy With Centro-Temporal Spikes Benign Epilepsy Of Childhood With Centrotemporal Spikes Benign Epilepsy With Centrotemporal Spikes Benign Rolandic Epilepsy of Childhood Centralopathic Epilepsies Centralopathic Epilepsy Centrotemporal Epilepsies Centrotemporal Epilepsy Epilepsies, Centralopathic Epilepsies, Centrotemporal Epilepsies, Temporal-Central Focal Epilepsy, Benign Rolandic Epilepsy, Centralopathic Epilepsy, Centrotemporal Epilepsy, Temporal-Central Focal Focal Epilepsies, Temporal-Central Focal Epilepsy, Temporal-Central Rolandic Epilepsy, Benign Temporal Central Focal Epilepsy Temporal-Central Focal Epilepsies Temporal-Central Focal Epilepsy |
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