How is Lennox-Gastaut syndrome treated?
How is Lennox-Gastaut syndrome treated?
The three main forms of treatment of Lennox-Gastaut syndrome are anti-epileptic drugs (AEDs), dietary therapy (typically the ketogenic diet) or device/surgery (VNS therapy or corpus callosotomy). Rarely, resective surgery is an option. Treatment may require the coordinated efforts of a team of specialists.
Is Lennox-Gastaut syndrome life limiting?
While we were unable to locate data describing a life expectancy, the mortality rate associated with Lennox-Gastaut syndrome ranges from 3 to 7%. People with Lennox-Gastaut syndrome have an increased risk of death compared to their peers of the same age.
Can atonic seizures be cured?
These types of seizures generally first occur in childhood, and they may extend into adulthood. Although there is no cure for atonic seizures, some treatments help manage the symptoms. People may also be able to prevent some seizures by identifying and avoiding triggers.
What is intractable Lennox-Gastaut Syndrome?
Lennox-Gastaut syndrome (LGS) is a type of epilepsy. Patients with LGS experience many different types of seizures including: Tonic – stiffening of the body. Atonic – temporary loss of muscle tone and consciousness, causing the patient to fall.
What is lgs?
What is LGS?
What is the most rare epilepsy?
Dravet syndrome is a rare, drug-resistant epilepsy that begins in the first year of life in an otherwise healthy infant. It is lifelong. It usually presents with a prolonged seizure with fever that affects one side of the body. Most cases are due to severe SCN1A gene mutations.
What is the prognosis of Lennox-Gastaut syndrome (LGS)?
The prognosis for individuals with Lennox-Gastaut syndrome varies. There is no cure for the disorder. Complete recovery , including freedom from seizures and normal development, is very rare.
What is the prevalence of Lennox-Gastaut syndrome (LGS)?
The prevalence of LGS is estimated between 1 and 2% of all patients with epilepsy. The etiology of LGS is often divided into two groups: identifiable (genetic-structural-metabolic) in 65 to 75% of the patients and LGS of unknown cause in others. Lennox-Gastaut syndrome may be considered as secondary network epilepsy.
What is Lennox-Gastaut syndrome (LGS)?
What Is Lennox-Gastaut Syndrome? Lennox-Gastaut syndrome ( LGS) is a rare and severe kind of epilepsy that starts in childhood. Children with LGS have seizures often, and they have several different kinds of seizures. This condition is hard to treat, but researchers are looking for new therapies.
