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Affected individuals generally exhibit motor control problems or other developmental delays, and they often develop cerebral palsy or epilepsy later in life. The white matter in preterm born children is particularly vulnerable during the third trimester of pregnancy when white matter developing takes place and the myelination process starts ...
They may persist beyond infancy, or, rarely, commence only later in childhood. Many individuals with the syndrome go on to develop other forms of epilepsy later in life (notably Lennox–Gastaut syndrome), and persisting neurodevelopmental deficits are common; [2] notably, up to about a third of children are subsequently diagnosed with autism. [6]
Anything that causes epilepsy causes epileptogenesis, because epileptogenesis is the process of developing epilepsy. Structural causes of epilepsy include neurodegenerative diseases , traumatic brain injury , stroke , brain tumor , infections of the central nervous system , and status epilepticus (a prolonged seizure or a series of seizures ...
[2] [3] However, some studies have reported that a minority of children with BFNS consequently develop intellectual disability. [3] Additionally, BFNS increases lifetime susceptibility to seizures as approximately 14% of those afflicted go on to develop epilepsy later in life. [4]
Also known as Janz syndrome, juvenile myoclonic epilepsy (JME) is a common form of epilepsy, accounting for ~10% of all cases and ~25% of cases of idiopathic generalized epilepsies. Many children with CAE go on to develop JME. JME first presents between the ages of 12 and 18 with prominent myoclonic seizures.
A woman whose lifelong dream of becoming a paramedic was shattered by a shock epilepsy diagnosis aged 21 when she “had a seizure and lost everything” has since found a “new norm” with a ...