Juvenile Myoclonic Epilepsy (JME) Home A-Z Health Information A-Z Health Library Juvenile Myoclonic Epilepsy (JME) Overview Juvenile myoclonic epilepsy (JME), also known as Janz syndrome, is a type of generalised epilepsy syndrome usually seen in young females in their second or third decades. It is characterised by different types of seizures afflicting the same individuals. Symptoms People with JME may experience different kinds of seizures:Myoclonic seizures are the hallmark of JME. They are sudden jerk-like movements of extremities, usually after getting up from sleep or while going to sleep. They occur in cluster with many jerks happening continuously and may vary from mild to severe in intensity. They may manifest as sudden dropping of objects from hands or frank jerks.Generalised tonic-clonic seizures are full-blown convulsions (muscle contraction and relaxation repeatedly) with abnormal posturing and jerking of the body. In JME, it is typically seen following clusters of myoclonic jerks.Absence seizures may also be seen in JME with the above-mentioned seizures. The patient suddenly becomes blank and discontinues all activities. After a brief interval, they begin to resume their activity without any awareness about the episode.Photosensitivity: The seizure attacks may get precipitated by bright flickering or flashing lights, as in video games. Causes The exact cause remains unknown. Genetics may play a role, as JME sometimes runs in families. You may be at higher risk of JME if you have:Family historyAge of onset: JME usually begins between ages 12 and 18.Male sexCommon triggers for JME include:Lack of sleepExtreme tirednessStressAlcohol consumptionFlickering lights, such as strobe lights, video games, or light reflecting off ocean waves or snowMenstrual periods for some girls and women Diagnostics Doctors may use the following to diagnose JME:Clinical history: Doctors may use the following to diagnose JME:EEG (electroencephalogram): shows a typical pattern of 3-6 Hz generalised spike and wave activity with photosensitivityMRI scan: Usually normal, but may be done to rule out structural causesGenetic testing: Sometimes done, though not always required Treatment JME can usually be well controlled with treatment:Antiseizure medications: JME can usually be well controlled with treatment:Lifestyle modifications: Avoid precipitating factors such as sleep deprivation, stress, poor drug compliance, stimulant drugs, and alcohol When to see a doctor? You should see a doctor if you:Experience sudden unexplained jerks, especially in the morningHave episodes of blank staring or unresponsivenessSuffer from convulsions or repeated seizure-like eventsNotice seizures triggered by flashing lights or lack of sleep Prevention While JME cannot be prevented completely, seizures can often be avoided by:Maintaining regular sleep patternsManaging stress and fatigueMinimising exposure to flashing lights or screens Specialist to approach For diagnosis and management of JME, consult a Neurologist (specialist in brain and nerve disorders) Disclaimer: The information in this Health Library is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare professional with any questions about a medical condition or before starting any treatment. Use of this site and its content does not establish a doctor–patient relationship. In case of a medical emergency, call your local emergency number or visit the nearest emergency facility immediately.