Other terms
Benign Neonatal Epilepsies,Benign Neonatal Epilepsy,Epilepsies, Benign Neonatal,Neonatal Epilepsies, Benign,Neonatal Epilepsy, Benign,Neonatal Convulsions, Benign,Benign Neonatal Convulsion,Benign Neonatal Convulsions,Convulsion, Benign Neonatal,Convulsions, Benign Neonatal,Neonatal Convulsion, Benign,Benign Familial Neonatal Epilepsy,Familial Benign Neonatal Epilepsy,Epilepsy, Benign Neonatal, Familial,Familial Benign Neonatal Convulsions,Benign Familial Neonatal Convulsions,Convulsions, Benign Neonatal, Familial,Benign Neonatal Epilepsy, Nonfamilial,Benign Neonatal Non-Familial Convulsions,Benign Neonatal Non Familial Convulsions,Benign Neonatal Nonfamilial Epilepsy,Epilepsy, Benign Neonatal, Non-Familial,Epilepsy, Benign Neonatal, Nonfamilial,Non-Familial Benign Neonatal Epilepsy,Non Familial Benign Neonatal Epilepsy,Non-Familial Benign Neonatal Convulsions,Non Familial Benign Neonatal Convulsions,Convulsions, Benign Neonatal, Non-Familial,Benign Non-Familial Neonatal Convulsions,Benign Non Familial Neonatal Convulsions
Description
Epilepsy, Benign Neonatal: A condition marked by recurrent seizures that occur during the first 4-6 weeks of life despite an otherwise benign neonatal course. Autosomal dominant familial and sporadic forms have been identified. Seizures generally consist of brief episodes of tonic posturing and other movements, apnea, eye deviations, and blood pressure fluctuations. These tend to remit after the 6th week of life. The risk of developing epilepsy at an older age is moderately increased in the familial form of this disorder. (Neurologia 1996 Feb;11(2):51-5)
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