Types of epilepsy
There are many different types of epilepsy. Epileptologists (neurologists who specialize in epilepsy) classify epilepsies based on the types of seizures, what causes them, and other symptoms.
Developmental and epileptic encephalopathies (DEEs) are severe types of epilepsy that begin early in life, usually during infancy. DEEs are characterized by a combination of repeated seizures and encephalopathy (a condition affecting brain function).
Learn more about the Pediatric Epilepsy Program at Children’s Hospital of Philadelphia
Epilepsies that affect fewer than 200,000 people worldwide are considered rare. There are about two dozen types of rare epilepsy, including:
- Angelman syndrome is an inherited condition caused by abnormal changes in the UBE3A gene. Seizures usually begin in children with Angelman syndrome between 2 and 3 years of age.
- CDKL5 deficiency disorder is an inherited epilepsy that affects infants usually within the first three months of life. The condition is caused by changes in the CDKL5 gene that carries the code to make a protein needed for normal brain development.
- Pyridoxine-dependent epilepsy is an inherited epilepsy with seizures beginning in infancy and sometimes even before birth. These seizures respond well to supplemental treatment with pyridoxine (vitamin B6).
- Rasmussen syndrome is a type of chronic inflammation in which cells from the immune system damage only one side of the brain. This inflammatory damage causes seizures, cognitive and speech impairments, and problems moving one side of the body (hemiparesis). The condition usually occurs in children under 10.
- Tuberous sclerosis complex (TSC) is an inherited disorder that causes tumors with a root-shaped (tuberous) appearance in the brain. Epilepsy is common in people diagnosed with TSC.