Epilepsy syndromes
Epilepsy syndromes
Epilepsy syndromes (pronounced eh-puh-lep-see sin-drohmz) are a group of neurological disorders characterized by epileptic seizures. The etymology of the term "epilepsy" comes from the Greek word "epilēpsía," meaning "to seize, possess, or afflict."
Definition
Epilepsy syndromes are defined by a cluster of signs and symptoms customarily occurring together. These syndromes are typically characterized by the type, frequency, and cause of seizures, as well as age of onset, prognosis, and other neurological and behavioral features.
Classification
Epilepsy syndromes are classified into three main categories: generalized, focal, and combined generalized and focal epilepsy syndromes.
- Generalized epilepsy syndromes involve seizures that start from both sides of the brain at once.
- Focal epilepsy syndromes involve seizures that start from one area or group of cells in one side of the brain.
- Combined generalized and focal epilepsy syndromes involve both generalized and focal seizures.
Common Epilepsy Syndromes
Some of the most common epilepsy syndromes include:
- Juvenile Myoclonic Epilepsy (JME)
- Childhood Absence Epilepsy (CAE)
- Lennox-Gastaut Syndrome (LGS)
- Dravet Syndrome (DS)
- West Syndrome (WS)
Treatment
Treatment for epilepsy syndromes typically involves the use of antiepileptic drugs (AEDs). In some cases, ketogenic diet, vagus nerve stimulation (VNS), or epilepsy surgery may be recommended.
Prognosis
The prognosis for epilepsy syndromes varies widely, depending on the specific syndrome and other individual factors. Some syndromes are benign and outgrown with age, while others may be lifelong conditions.
See Also
External links
- Medical encyclopedia article on Epilepsy syndromes
- Wikipedia's article - Epilepsy syndromes
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