Dravet's syndrome; a catastrophic epileptic syndrome
Pakistan Pediatric Journal. 2013; 37 (4): 252-256
in English
| IMEMR
| ID: emr-139806
ABSTRACT
It was first described by Charlotte Dravet in 1978 and has been recognized as a syndrome by the International League Against Epilepsy since 1989. It starts in the first year of life frequently with febrile seizures [FS] in an, otherwise, normal infant. This is followed by refractory and mixed type of seizures. [Dravet's syndrome] [DS] previously named severe myoclonic epilepsy of infancy [SMEI], or epilepsy with polymorphic seizures. DS is caused by a mutation in the neuronal sodium channel gene, SCN1A, that is also mutated in generalized epilepsy with FS+ [GEFS+]
Search on Google
Index:
IMEMR (Eastern Mediterranean)
Main subject:
Seizures
/
Social Change
/
Magnetic Resonance Spectroscopy
/
Epilepsies, Myoclonic
/
Electroencephalography
/
Epilepsy
Type of study:
Case report
Limits:
Humans
/
Male
Language:
English
Journal:
Pak. Pediatr. J.
Year:
2013
Similar
MEDLINE
...
LILACS
LIS