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Dravet syndrome: a technologist's perspective.

Patricia A Lordeon1, Bilal Sitwat, Donna Brehm

  • 1Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.

American Journal of Electroneurodiagnostic Technology
|February 15, 2011
PubMed
Summary

Dravet Syndrome (DS), or Severe Myoclonic Epilepsy in Infancy (SMEI), is a rare genetic epilepsy causing frequent seizures and developmental regression in infants. Early recognition by EEG technologists is crucial for timely diagnosis and management.

Area of Science:

  • Pediatric Neurology
  • Clinical Electrophysiology
  • Genetics

Background:

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  • Dravet Syndrome (DS), also known as Severe Myoclonic Epilepsy in Infancy (SMEI), is a rare genetic epilepsy originating in infancy.
  • It is characterized by prolonged, generalized seizures, often initially triggered by fever, evolving into various seizure types.
  • Affected individuals typically experience normal early development followed by developmental regression.