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... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Epilepsy > Epileptic Syndromes > Epilepsy, Rolandic
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Epilepsy > Epilepsies, Partial > Epilepsy, Rolandic

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Epilepsy, Rolandic  

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Tipo

  • mesh:Descriptor

Definición

  • 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)

Concepto genérico

Etiquetas alternativas

  • Rolands Epilepsy
  • Sylvian Epilepsy

En otras lenguas

  • Épilepsie rolandique

    francés

  • Épilepsie à paroxysme rolandique
  • EPR (Épilepsie à Paroxysme Rolandique)

URI

http://data.loterre.fr/ark:/67375/JVR-JMFCT1NQ-G

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