Lennox-Gastaut Syndrome
Lennox-Gastaut syndrome is a rare, debilitating form of epilepsy that causes seizures, cognitive impairment and abnormal brain activity.
What is Lennox-Gastaut Syndrome?
Lennox-Gastaut syndrome is a rare and often debilitating type of epilepsy that usually first appears between the ages of 2 and 6. Due to its unique combination of symptoms, this condition is one of the most challenging forms of epilepsy to treat. What’s more, Lennox-Gastaut syndrome is a dangerous condition due to the frequent falls, injuries and cognitive (thinking) impairment that can impact the child’s quality of life.
What are the signs and symptoms of Lennox-Gastaut Syndrome?
- Mood instability
- Personality disturbances
- Poor social skills and attention seeking behavior
- Seizures
What are the causes of Lennox-Gastaut Syndrome?
In 20 to 30 percent of cases, there is no known cause of this condition. Some of the known causes of Lennox-Gastaut syndrome include:
- Brain injury associated with pregnancy or birth, such as asphyxia, low birth weight or prematurity
- Developmental malformations of the brain
- Certain metabolic conditions
- Severe brain infections, such as encephalitis, meningitis or rubella
Lennox-Gastaut Syndrome Doctors and Providers
-
Rana Said, MD Professor of Pediatrics and Neurology -
Alison Dolce, MD Pediatric Neurologist -
Andrea Lowden, MD Pediatric Neurologist -
Deepa Sirsi, MD Pediatric Neurologist