Kids with juvenile myoclonic epilepsy have myoclonic seizures that usually begin during the teen years. They may also have absence seizures and generalized tonic-clonic seizures.
Seizures may happen less often in adulthood, but medicine will likely be needed for life.
Different types of seizures can happen in juvenile myoclonic (my-uh-KLON-ik) epilepsy. The types and their symptoms are:
This kind of seizure is the most common type in juvenile myoclonic epilepsy, and is the hallmark of this condition. In a myoclonic seizure, a child:
An absence seizure starts suddenly in the middle of activity and ends abruptly. During the seizure, a child:
In this type of seizure, a child:
Seizures in juvenile myoclonic epilepsy typically happen within 30 minutes of waking up in the morning or after a nap. They're more likely to happen when someone is tired, stressed, or didn't get enough sleep.
The cause of juvenile myoclonic epilepsy isn't known, but it tends to run in families. Genetic changes (mutations) have been associated with the condition.
If your child had a seizure, the doctor probably will want you to see a pediatric neurologist (a doctor who treats brain, spine, and nervous system problems). The neurologist will ask questions about what happened during the seizure, do an exam, and order an EEG to measure brain wave activity.
Seizures are usually well-controlled with medicine, which many people will need to take for life. If they’re not, doctors have other treatments to try.
To help your child live better with epilepsy, be sure they follow the neurologist’s recommendations about:
To keep your child safe during a seizure, make sure that other adults and caregivers (family members, babysitters, teachers, coaches, etc.) know what to do.
Juvenile myoclonic epilepsy is a lifelong condition. But many kids go on to live a normal life with a few extra steps taken to keep them safe. When it's time, help your child successfully move to adult health care.
If your child has epilepsy, reassure them that they’re not alone. Your doctor and the care team can answer questions and offer support. They also might be able to recommend a local support group. Online organizations can help too, such as:
Note: All information is for educational purposes only. For specific medical advice, diagnoses, and treatment, consult your doctor.
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