KCNQ2 benign neonatal benign familial neonatal seizures

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KCNQ2 benign neonatal benign familial neonatal seizures

A rare (1:100,000 live births) neonatal condition which is characterised by focal or generalised tonic-clonic seizures involving both sides of the brai, which affects the entire body, causing muscle rigidity, convulsions and loss of consciousness. The seizures usually resolve by the fourth month of life, but some children have residual intellectual disability and myokimia (involuntary rippling of muscles).
 
Molecular pathology
Mutations in KCNQ2, less commonly in KCNQ3, both of which encode potassium channel proteins.
References in periodicals archive ?
Epilepsies of unknown cause Conditions with epileptic seizures that are traditionally not diagnosed as a form of epilepsy Benign neonatal seizures (BNS) Febrile seizures (FS) (a) The arrangement of electroclinical syndromes does not reflect etiology, (b) Sometimes referred to as Electrical Status Epilepticus during Slow Sleep (ESES), * Reference: Berg AT et al.

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