Is Lennox-Gastaut syndrome curable?

Is Lennox-Gastaut syndrome curable?

There is no cure for the disorder. Complete recovery, including freedom from seizures and normal development, is very rare. The prognosis for individuals with Lennox-Gastaut syndrome varies. There is no cure for the disorder.

Is Lennox-Gastaut syndrome fatal?

The progressive intellectual impairment associated with Lennox-Gastaut syndrome means that many patients require full-time care throughout life. The short-term mortality of Lennox-Gastaut syndrome is approximately 4-7%. This is largely due to seizure-related fatal accidents.

How bad is Lennox-Gastaut syndrome?

Lennox-Gastaut syndrome (LGS) is a severe form of childhood epilepsy with multiple types of seizures. In 1 out of 4 people, no cause can be found. About 2 to 5% of children with epilepsy have LGS. Usually, LGS persists through childhood and adolescence to adult years.

Are you born with Lennox-Gastaut syndrome?

Symptomatic Lennox-Gastaut syndrome can be caused by a number of factors, including a brain injury at or around birth, a brain malformation or an infection of the central nervous system. Lennox-Gastaut syndrome may be treated with medications, certain diets and, in some cases, surgery.

What is the most severe form of epilepsy?

Tonic-clonic seizures. Tonic-clonic seizures, previously known as grand mal seizures, are the most dramatic type of epileptic seizure. They can cause an abrupt loss of consciousness and body stiffening, twitching and shaking. They sometimes cause loss of bladder control or biting your tongue.

How long can you live with Lennox-Gastaut syndrome?

We investigated the long-term prognosis of Lennox-Gastaut syndrome (LGS) in 72 patients followed up for > 10 years. Long-term seizure and intellectual outcomes were poor, as previously reported. The diagnosis of LGS was first made in the age range from 2 to 15 years with peak occurrence at 5 years.

Does epilepsy shorten your life?

Reduction in life expectancy can be up to 2 years for people with a diagnosis of idiopathic/cryptogenic epilepsy, and the reduction can be up to 10 years in people with symptomatic epilepsy. Reductions in life expectancy are highest at the time of diagnosis and diminish with time.

Who gets Lennox-Gastaut Syndrome?

LGS is most common in children between the ages of 2 and 7 years old. Boys are slightly more likely to be affected than girls. In most cases the cause for LGS is known.