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GENATLAS PHENOTYPE

last update : 27/06/2006

Symbol	EBN2
Location	8q24
Name	benign familial neonatal convulsions, 2
Other name(s)	epilepsy, benign familial neonatal, seizures, benign familial neonatal
Corresponding gene	KCNQ3
Other symbol(s)	BFNC
Main clinical features	characterized by frequent,brief seizures on or after the second day of life which often disappear spontaneously within a few weeks not associated with myokymia
Genetic determination	autosomal dominant
Function/system disorder	neurology
Type	disease

Gene product

Name	potassium voltage channel, Q subfamily, member 3, KCNQ3

Remark(s)