MeSH Browser

MeSH Heading: Epilepsy, Rolandic
Tree Number(s): C10.228.140.490.360.280; C10.228.140.490.493.250
Unique ID: D019305
RDF Unique Identifier: http://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)
Entry Term(s): BCECTS; BECTS; 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 Epilepsy; Centrotemporal Epilepsy; Epilepsy, Centrotemporal; Rolands Epilepsy; Sylvian Epilepsy; Temporal-Central Focal Epilepsy
Previous Indexing: Epilepsy, Partial (1986-1996)
Public MeSH Note: 1997
History Note: 1997
Date Established: 1997/01/01
Date of Entry: 1996/06/13
Revision Date: 2017/02/24

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urine (UR)

veterinary (VE)

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Epilepsy, Rolandic MeSH Descriptor Data 2025