"Epilepsy, Rolandic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
| Descriptor ID |
D019305
|
| MeSH Number(s) |
C10.228.140.490.360.280
|
| Concept/Terms |
Epilepsy, Rolandic- Epilepsy, Rolandic
- Epilepsies, Rolandic
- Rolandic Epilepsies
- Rolandic Epilepsy
- Rolands Epilepsy
- Epilepsy, Rolands
- Sylvian Epilepsy
- Epilepsy, Sylvian
Benign Rolandic Epilepsy- Benign Rolandic Epilepsy
- Epilepsy, Benign Rolandic
- Rolandic Epilepsy, Benign
- BECTS
- Benign Childhood Epilepsy With Centro-Temporal Spikes
- Benign Childhood Epilepsy With Centro Temporal Spikes
- Benign Epilepsy Of Childhood With Centrotemporal Spikes
- Temporal-Central Focal Epilepsy
- Benign Rolandic Epilepsy of Childhood
- Centralopathic Epilepsy
- Centralopathic Epilepsies
- Epilepsies, Centralopathic
- Epilepsy, Centralopathic
- Centrotemporal Epilepsy
- Epilepsy, Centrotemporal
- Centrotemporal Epilepsies
- Epilepsies, Centrotemporal
- BCECTS
- Benign Epilepsy With Centrotemporal Spikes
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Below are MeSH descriptors whose meaning is more general than "Epilepsy, Rolandic".
Below are MeSH descriptors whose meaning is more specific than "Epilepsy, Rolandic".
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