Dravet syndrome: inroads into understanding epileptic encephalopathies

J Pediatr. 2011 Mar;158(3):354-9. doi: 10.1016/j.jpeds.2010.10.035. Epub 2010 Dec 15.

Author

Richard P Morse¹

Affiliation

¹ Section of Neurology and Development, Department of Pediatrics, Children's Hospital at Dartmouth, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, NH 03756, USA. [email protected]

PMID: 21163495
DOI: 10.1016/j.jpeds.2010.10.035

No abstract available

MeSH terms

Child, Preschool
Developmental Disabilities* / diagnosis
Developmental Disabilities* / genetics
Developmental Disabilities* / physiopathology
Developmental Disabilities* / therapy
Epilepsies, Myoclonic* / diagnosis
Epilepsies, Myoclonic* / genetics
Epilepsies, Myoclonic* / physiopathology
Epilepsies, Myoclonic* / therapy
Genetic Predisposition to Disease
Humans
Infant
Infant, Newborn
NAV1.1 Voltage-Gated Sodium Channel
Nerve Tissue Proteins / genetics
Sodium Channels / genetics
Syndrome

Substances

NAV1.1 Voltage-Gated Sodium Channel
Nerve Tissue Proteins
SCN1A protein, human
Sodium Channels