Orphanet: Rolandic epilepsy speech dyspraxia syndrome
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Rolandic epilepsy-speech dyspraxia syndrome

Disease definition

Rolandic epilepsy-speech dyspraxia syndrome is a rare, genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.

ORPHA:163721

  • Synonym(s): -
  • Prevalence: -
  • Inheritance: Autosomal dominant or X-linked dominant 
  • Age of onset: -
  • ICD-10: -
  • OMIM: 245570  300643
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

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