Cognitive development in children with Dravet syndrome

Epilepsia

Volumn 52, Issue SUPPL. 2, 2011, Pages 39-43

  Ragona, Francesca ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

Development; Epilepsy; SCN1A mutation; SMEI

Indexed keywords

SODIUM CHANNEL NAV1.1;

ARTICLE; CHILD; CLINICAL ARTICLE; COGNITIVE DEVELOPMENT; DISEASE ASSOCIATION; FOLLOW UP; GENE MUTATION; GENETIC PREDISPOSITION; HUMAN; INFANT; MULTICENTER STUDY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSPECTIVE STUDY; RETROSPECTIVE STUDY; SEIZURE; SEVERE MYOCLONIC EPILEPSY IN INFANCY;

CHILD; CHILD DEVELOPMENT; COGNITION DISORDERS; EPILEPSIES, MYOCLONIC; FOLLOW-UP STUDIES; HUMANS; MULTICENTER STUDIES AS TOPIC; RETROSPECTIVE STUDIES; SYNDROME;

EID: 79953701098     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2011.03000.x     Document Type: Article

References (15)

1. Akiyama M, Kobayashi K, Yoshinaga H, Ohtsuka Y,. (2010) A long-term follow-up study of Dravet syndrome up to adulthood. Epilepsia 51: 1043-1052.
2. Caraballo RH, Fejerman N,. (2006) Dravet syndrome: a study of 53 patients. Epilepsy Res 70: 231-238.
3. Cassé-Perrot C, Wolff M, Dravet C,. (2001) Neuropsychological aspects of severe myoclonic epilepsy in infancy. In, Jambaque I, Lassonde M, Dulac O, (Eds) Neuropsychology of childhood epilepsy. Kluwer Academic/Plenum Publishers, New York, pp. 131-140.
4. Ceulemans BP, Claes LR, Lagae LG,. (2004) Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy. Pediatr Neurol 30: 236-243. (Pubitemid 38490433)
5. Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P,. (2001) De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet 68: 1327-1332. (Pubitemid 32510608)
6. Commission on Classification and terminology of the International League Against Epilepsy. (1989) Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 30: 389-399.
7. Dalla Bernardina B, Capovilla G, Chiamenti C,. (1987) Myoclonic Epilepsies of Infancy and Early Childhood: Nosological and Prognostic Approach. In, Wolf P, Darn M, Janz D, Dreifuss FE, (Eds) Advances in Epileptology. Raven Press, New York, pp. 175-179.
8. Dravet C,. (1978) Les épilepsies graves de l'enfant. Vie Méd 8: 543-548.
9. Dravet C, Roger J, Bureau M, Dalla Bernardina B,. (1982) Myoclonic epilepsy in childhood. In, Akimoto H, Kazamarsuri H, Seino M, Ward A, (Eds) Advances in epileptology: XIII Epilepsy International Symposium. Raven Press, New York, pp. 135-141.
10. Engel J Jr,. (2001) ILAE Commission Report. A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: Report of the ILAE task force on classification and terminology. Epilepsia 42: 796-803. (Pubitemid 32605946)
11. Ohmori I, Ouchida M, Ohtsuka Y, Oka E, Shimizu K,. (2002) Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy. Biochem Biophys Res Commun 295: 17-23. (Pubitemid 34743768)
12. Ragona F, Brazzo D, De Giorgi I, Morbi M, Freri E, Teutonico F, Gennaro E, Zara F, Binelli S, Veggiotti P, Granata T,. (2010) Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients. Brain Dev 32: 71-77.
13. Ragona F, Granata T, Dalla Bernardina B, Offredi F, Darra F, Battaglia D, Morbi M, Brazzo D, Cappelletti S, Chieffo D, De Giorgi I, Fontana E, Freri E, Marini C, Toraldo A, Specchio N, Veggiotti P, Vigevano F, Guerrini R, Guzzetta F, Dravet C,. (2011) Cognitive development in Dravet syndrome: a retrospective, multi center study of 26 patients. Epilepsia 52, 386-392.
14. Wallace RH, Hodgson BL, Grinton BE, Gardiner RM, Robinson R, Rodriguez-Casero V, Sadleir L, Morgan J, Harkin LA, Dibbens LM, Yamamoto T, Andermann E, Mulley JC, Berkovic SF, Scheffer IE,. (2003) Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms. Neurology 61: 765-769. (Pubitemid 37174470)
15. Wolff M, Cassé-Perrot C, Dravet C,. (2006) Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings. Epilepsia 47 (suppl 2): 45-48. (Pubitemid 44684620)