Familial benign neonatal epilepsy

BACKGROUND Benign familial neonatal convulsions (BFNC) is a rare autosomal dominant seizure disorder usually described to be… (More)

OBJECTIVES Infantile hemangiomas are the most common tumor of infancy. Risk factors for complications and need for treatment have… (More)

Benign familial neonatal convulsions (BFNC) is a rare autosomal dominant generalized epilepsy of the newborn infant. Seizures… (More)

The muscarinic-regulated potassium current (M-current), formed by the heteromeric assembly of subunits encoded by the KCNQ2 and… (More)

KCNQ2 and KCNQ3 are two homologous K(+) channel subunits that can combine to form heterotetrameric channels with properties of… (More)

Benign familial neonatal convulsions (BFNC) is an autosomal dominant epilepsy of infancy, with loci mapped to human chromosomes… (More)

Idiopathic generalized epilepsies account for about 40% of epilepsy up to age 40 and commonly have a genetic basis. One type is… (More)

Epilepsy affects more than 0.5% of the world's population and has a large genetic component. It is due to an electrical… (More)

Benign familial neonatal convulsions (BFNC), a class of idiopathic generalized epilepsy, is an autosomal dominantly inherited… (More)

The syndrome of benign familial neonatal convulsions (BFNC) is a rare autosomal dominant disorder characterized by unprovoked… (More)