Can you grow out of juvenile myoclonic epilepsy?

Juvenile Myoclonic Epilepsy Treatment Most patients with JME do not outgrow their seizures and will need to take medication for the rest of their lives. Individuals are encouraged to get enough sleep and avoid alcohol to reduce the likelihood of seizures.

Is juvenile myoclonic epilepsy rare?

Juvenile myoclonic epilepsy affects an estimated 1 in 1,000 people worldwide. Approximately 5 percent of people with epilepsy have juvenile myoclonic epilepsy.

What do you need to know about juvenile myoclonic epilepsy?

Juvenile Myoclonic Epilepsy. Generalized tonic-clonic seizures occur in nearly all people with JME. The cause is predominantly genetic. An EEG is the most important way to diagnose JME. Seizure medication often controls seizures well. People need to take seizure medicine throughout their life.

Can you have tonic clonic seizures with myoclonic epilepsy?

Progressive myoclonic epilepsy: The rare syndromes in this category feature a combination of myoclonic seizures and tonic-clonic seizures. Treatment is usually not successful for very long, as the patient deteriorates over time. Who is at risk for myoclonic seizures?

How long does myoclonic epilepsy take to remit?

Clinical context. Seizures remit within 6 months to 5 years from onset but generalized tonic-clonic seizures may be seen in teenage years in 10-20% of patients. Patients with photosensitivity may have seizures that are more difficult to control. Males are twice as likely to be affected as females. Antecedent and birth history is unremarkable.

When do myoclonic seizures occur in the face?

It begins in early childhood. The myoclonic seizures usually involve the neck, shoulders, upper arms, and often the face. They may be quite strong and are difficult to control. Progressive myoclonic epilepsy: The rare syndromes in this category feature a combination of myoclonic seizures and tonic-clonic seizures.