Ads
related to: what causes juvenile myoclonic epilepsy- Epilepsy
Learn About Medical & Surgical
Treatment Options Available
- Virtual Epilepsy Care
Virtual Care Regardless of Location
Receive Comprehensive Epilepsy Care
- Generalized Seizures
Access a Free Treatment Guide.
Learn More About Seizures.
- Focal Seizures
Access a Free Treatment Guide.
Learn More About Seizures.
- Epilepsy
Search results
Results from the WOW.Com Content Network
Juvenile myoclonic epilepsy (JME), also known as Janz syndrome or impulsive petit mal, is a form of hereditary, idiopathic generalized epilepsy, [1] representing 5–10% of all epilepsy cases.
Juvenile myoclonic epilepsy (JME) is a prevalent and typical form of idiopathic generalized epilepsy (IGE) syndrome. However, establishing a precise definition for JME has posed difficulties, making it equally challenging to establish clear indicators for predicting its course and results.
Also known as Janz syndrome, juvenile myoclonic epilepsy (JME) is a common form of epilepsy, accounting for ~10% of all cases and ~25% of cases of idiopathic generalized epilepsies. Many children with CAE go on to develop JME. JME first presents between the ages of 12 and 18 with prominent myoclonic seizures.
Essential myoclonus tends to be stable without increasing in severity over time. Some scientists speculate that some forms of essential myoclonus may be a type of epilepsy with no known cause. Juvenile myoclonic epilepsy (JME) usually consists of jerking and muscle twitches of the upper extremities. This may include the arms, shoulders, elbows ...
The main component setting PME apart from other forms of epilepsy is progressive deterioration and resistance to treatment. [2] Therefore, in the early stages of PME the symptoms and EEG may appear like Generalized epilepsy, Juvenile myoclonic epilepsy, benign childhood myoclonic epilepsy, and Huntington's disease. [3]
Stress can induce seizures in people with epilepsy, and is a risk factor for developing epilepsy. Severity, duration, and time at which stress occurs during development all contribute to frequency and susceptibility to developing epilepsy. It is one of the most frequently self-reported triggers in patients with epilepsy. [48] [49]
Ads
related to: what causes juvenile myoclonic epilepsy