KCNQ2-related epileptic encephalopathy

Engelsk navn: KCNQ2-related epileptic encephalopathy
Engelske synonym: KCNQ2-NEE,KCNQ2-related neonatal epileptic encephalopathy


KCNQ2-related epileptic encephalopathy is a severe form of neonatal epilepsy that usually manifests in newborns during the first week of life with seizures (that affect alternatively both sides of the body), often accompanied by clonic jerking or more complex motor behavior, as well as signs of encephalopathy such as diffuse hypotonia, limb spasticity, lack of visual fixation and tracking and mild to moderate intellectual deficiency. The severity can range from controlled to intractable seizures and mild/moderate to severe intellectual disability.

Fra Orphanet

ORPHA: 439218
Klassifiseringsnivå: Disorder
ICD-10: G40.4

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