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Self-limited neonatal seizures

MONDO:0800479

A neonatal/infantile epilepsy syndrome where seizures start in the neonate between day 4 and 7 of life and are often unilateral clonic events that recur and may alternate sides from seizure to seizure. Seizures can be repetitive over hours to days. Seizures remit by 4-6 months of age. A proportion of those affected may have seizures in later life. The child is expected to have normal developmental progress. This is distinguished from familial neonatal epilepsy on the basis of family history. These entities may have similar genetic etiologies, with de novo mutations responsible for the lack of family history in self-limited neonatal seizures.

Also known as: SeLNE

6 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Epilepsy (398) Nervous system disorder (217) Brain disorder (110) Central nervous system disorder (97) Human disease (14) Epilepsy syndrome (2) Neonatal/infantile epilepsy syndrome (1) Disease by body system or component (0) Neonatal/infantile-onset self-limited epilepsy syndrome (0)
Trials to join now! 3 Not yet finished but already full! 3
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