Benign neonatal seizures

From Wikipedia, the free encyclopedia
Jump to: navigation, search

Benign neonatal seizures are somewhat rare syndromes (medical problems) which cause seizures in newborn infants. A seizure is caused by problems in the electrical activity in the brain.

One syndrome is Benign idiopathic neonatal seizures (BINS) and the other is Benign familial neonatal seizures (BFNS). Both syndromes usually happen in infants in the neonatal period, which is the first 28 days after birth. In most cases, the first seizure happens within the first few days after birth. However, some infants may have their first seizure later in the neonatal period, or even months after the neonatal period. The last seizure usually happens while the infant is still in the neonatal period, but seizures may continue after this time.[1]

A third syndrome called benign familial neonatal-infantile syndrome (BFNIS). It may cause the first seizure between the second day upwards to 6 months after birth, and usually stops within the first 12 months.

These syndromes are called "benign" because they usually cause no long-term harm to the infant, but there is a greater chance of getting seizures later in life.

In Benign idiopathic neonatal seizures the cause is not known (this is what the word "idiopathic" means). In Benign familial neonatal seizures and Benign familial neonatal-infantile seizures, there is a genetic mutation, which means a change in the genes that an infant gets from their parents.[2] These disorders are inherited (they "run in the family"). This is what the word "familial" means.

Electrical charges inside the human brain
The human brain works on small amounts of electrical charges. Problems with these electrical charges (like too much electrical charge) may cause a seizure.

References[change | change source]

  1. Epileptic Syndromes in Infancy, Childhood, and Adolescence. Ed. Joseph Roger, Michelle Bureau, Charlotte Dravet, Pierre Genton. John Libbey Eurotext Ltd; 4th edition (March 6, 2006)ISBN-10: 2742005692 pp. 1-14
  2. Madia, F., P. Striano, E. Gennaro, M. Malacarne, R. Paravidino, R. Biancheri, M. Budetta et al. "Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy." Neurology 67, no. 7 (2006): 1230-1235.