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Benign Rolandic epilepsy (medical condition): A benign form of childhood epilepsy that tends to occur...more »
See also:
Centrotemporal epilepsy:
»Introduction: Centrotemporal epilepsy
»Symptoms of Centrotemporal epilepsy
Benign Rolandic epilepsy: 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. The episodes tend to occur at night and may become secondarily generalized. In most cases, affected children are neurologically and developmentally normal. The electroencephalogram shows characteristic high-voltage sharp waves over the central temporal regions, which are more prominent during drowsiness and sleep. In general, seizures do not continue beyond mid-adolescence. (From Epilepsia 1998 39;Suppl 4:S32-S41)
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Benign Rolandic epilepsy:
Benign Rolandic epilepsy: Another name for Centrotemporal epilepsy (or close medical condition association).
»Introduction: Centrotemporal epilepsy
»Symptoms of Centrotemporal epilepsy
Benign Rolandic epilepsy: Benign Rolandic epilepsy is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Benign Rolandic epilepsy incude:
Read more about symptoms of Benign Rolandic epilepsy (Centrotemporal epilepsy)
Source: Diseases Database
Source: Diseases Database
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