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|Title: ||Clinical correlations of mutation in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy|
|Authors: ||Ceulemans, B.|
|Issue Date: ||2004|
|Publisher: ||ELSEVIER SCIENCE INC|
|Citation: ||Pediatric neurology, 30(4). p. 236-243|
|Abstract: ||Mutations in the alpha-subunit of the first neuronal sodium channel gene SCNIA have been described in isolated patients with severe myoclonic epilepsy in infancy or Dravet syndrome and in families with generalized epilepsy with febrile seizures plus. To rind phenotype/genotype correlations, we reviewed all published cases of mutations in SCNIA in addition to four new patients reported here. A total of 60 mutations were observed. Approximately 52% (31/60) are truncating mutations correlating with de novo cases of classical Dravet syndrome in 32 of 34 (94%) patients. Missense mutations in the pore-forming part constitute 27% (16/60) and correspond to a classical type in 12 of 16 (75%) patients. Missense mutations in the voltage sensor were present in 12% (7/60) and correlate with a clinical picture ranging from febrile seizures plus to severe myoclonic epilepsy in infancy. Outside these regions missense mutations are rare and account for only 10% (6/60), corresponding mostly with febrile seizures plus. These results illustrate that the clinical spectrum of SCN1A mutations ranges from febrile seizures, febrile seizures plus, over a milder type to the classical form of severe myoclonic epilepsy in infancy, and confirm the clinical experience that severe myoclonic epilepsy in infancy is the most severe form on this spectrum. (C) 2004 by Elsevier Inc. All rights reserved.|
|ISI #: ||000221138700002|
|Type: ||Journal Contribution|
|Appears in Collections: ||Research publications|
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