Juvenile Myoclonic Epilepsy
What Is Juvenile Myoclonic Epilepsy?
Seizures may happen less often in adulthood, but medicine will likely be needed for life.
What Are the Signs & Symptoms of a Juvenile Myoclonic Seizure?
Different types of seizures can happen in juvenile myoclonic (my-uh-KLON-ik) epilepsy. The types and their symptoms are:
In a myoclonic seizure, a child:
- has brief muscle twitches or jerks in the upper arms, shoulders, or neck
- has movements on both sides of the body at the same time
- usually is awake and can think clearly during and right after the seizure
An absence seizure starts suddenly in the middle of activity and ends abruptly. During the seizure, a child:
- "blanks out" or has staring spells that last 5–20 seconds
- may flutter their eyes or look upward
- is unaware of what is going on during the seizure
- returns to normal activity and won't remember having the seizure after it’s over
In this type of seizure, a child:
- has convulsions, or rigid muscles and rhythmic body jerks
- rolls the eyes back
- cries out
- may pee or poop
- can't respond during seizure
- is confused and sleepy after the seizure
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 or stressed.
What Causes Juvenile Myoclonic Epilepsy?
Juvenile myoclonic epilepsy is mainly caused by genetic changes (mutations). It tends to run in families.
How Is Juvenile Myoclonic Epilepsy Diagnosed?
If a child has a seizure, doctors will look for a cause. Kids who’ve had a seizure might need to see a pediatric neurologist (a doctor who treats brain, spine, and nervous system problems). Tests can include:
- EEG to measure brain wave activity.
- VEEG, or video electroencephalography (EEG with video recording)
- CAT scans or MRI scans to get very detailed images of the brain and to rule out other causes of the seizures
How Is Juvenile Myoclonic Epilepsy Treated?
Seizures are usually well controlled with medicine. If they’re not, doctors have other treatments to try.
How Can Parents Help?
To help your child live better with epilepsy, be sure they follow the neurologist’s recommendations about:
- taking any medicines
- avoiding triggers (such as excessive stress, lack of sleep, blinking lights, drinking alcohol, some types of medicines)
- taking precautions while swimming or bathing
- whether it’s OK for your teen to drive
- whether your child should wear a medical ID bracelet
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. When it's time, help your child successfully move to adult health care.
What Else Should I Know?
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:
- Temporal Lobe Epilepsy
- First Aid: Seizures
- Brain and Nervous System
- Epilepsy Surgery
- Benign Rolandic Epilepsy
- Absence Seizures
- Intractable Epilepsy
- Epilepsy Factsheet (for Schools)