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Nonfunctional SCN1A Is Common in Severe Myoclonic Epilepsy of Infancy

✍ Scribed by Iori Ohmori; Kristopher M. Kahlig; Thomas H. Rhodes; Dao W. Wang; Alfred L. George Jr


Book ID
109109021
Publisher
Wiley (Blackwell Publishing)
Year
2006
Tongue
English
Weight
289 KB
Volume
47
Category
Article
ISSN
0013-9580

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Severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) is a rare disorder occurring in young children often without a family history of a similar disorder. The earliest disease manifestations are usually fever-associated seizures. Later in life, patients display different types of afebrile s