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When Should Clinicians Order Genetic Testing for Dravet Syndrome?

  • Published:2011-11 Issue:5 Volume:45 Page:319-323
  • ISSN:0887-8994
  • Container-title:Pediatric Neurology
  • language:en
  • Short-container-title:Pediatric Neurology

Author:

Fountain-Capal Jamie K.,Holland Katherine D.,Gilbert Donald L.,Hallinan Barbara E.

Funder

Division of Neurology at the Cincinnati Children’s Hospital Medical Center

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference19 articles.

1. Les epilepsies graves de l’enfant;Dravet;Vie Med,1978

2. Myoclonic epilepsies in childhood;Dravet,1982

3. The spectrum of SCN1A-related infantile epileptic encephalopathies;Harkin;Brain,2007

4. Dravet syndrome (severe myoclonic epilepsy in infancy): A retrospective study of 16 patients;Korff;J Child Neurol,2007

5. Severe myoclonic epilepsy of infants (Dravet syndrome): Natural history and neuropsychological findings;Wolff;Epilepsia,2006

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