Genetic epileptic syndromes with neonatal onset

Definition

Epilepsy with onset in the first 30 days of life resulting from one or more known or presumed genetic defects in which seizures are the core symptom of the disorder.

Exclusions

• Epilepsy due to prenatal or perinatal brain insults (8A60.0)
• Neonatal seizures (KB06)

3 subordinate codes

• 8A61.00Pyridoxal dependent epilepsy
• 4B4YOther specified diseases of the immune system
• 4B4ZDiseases of the immune system, unspecified

Nearby in Genetic or presumed genetic syndromes primarily expressed as epilepsy

• 8A61.1Genetic epileptic syndromes with onset in infancy
• 8A61.2Genetic epileptic syndromes with childhood onset
• 8A61.3Genetic epileptic syndrome with adolescent or adult onset
• 8A61.4Genetic epileptic syndromes with variable age of onset
• 4B4YOther specified diseases of the immune system
• 4B4ZDiseases of the immune system, unspecified