On this page we are going to tell you a little bit more
information about Dravet Syndrome. Dravet Syndrome is a rare and devastating
form of epilepsy that begins in infancy. Its cause is a genetic mutation, but what causes that
mutation is unknown. It’s a fairly new illness so there isn’t much research
available about it.
Only one in 20,000 children is affected by it, which means that out of 500 children with epilepsy only
one is likely to have this form of epilepsy.
In addition to this the children
unlucky enough to have this form of epilepsy are faced with the fact that
Dravet Syndrome is one of the most resistant to epilepsy medications, some even aggravating the condition. Children
with Dravet Syndrome do not outgrow this condition, they are stuck with it for
life and it affects everything they do in their day to day lives.
The onset of the syndrome occurs in the first year of life
with prolonged seizures lasting anywhere from 5 minutes to an hour brought on
by fever or high temperatures. As the child
goes into its second year of life the seizures occur more frequently and do not
require a fever to be present. Some children can have over a 100 small seizures a day (little eye flutters that are shown as seizures on EEG) on top of having major seizures 4-5 times a week.
Due to the seizures becoming more frequent as the child gets
older, their development starts to get slower, especially between the ages of two
and four. This can often include regression or loss of developmental skills
such as speech and language; they can even lose their ability to control
movement.
As the child gets older the seizures continue to be very
difficult to control. Learning disabilities are usually severe and as it
progresses most children become unsteady on their feet. This requires them to
have constant care and supervision throughout their lives, which can be very
draining both emotionally and financially for families who care for the affected
individuals. Usually by the age of 14 or 16 years, the seizures tend to become
less frequent, although there is very little evidence of this in research due
to it being a recently discovered syndrome.
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