What is Juvenile Myoclonic Epilepsy? Juvenile myoclonic epilepsy (JME) is an epileptic condition that develops in children and adolescents, invariably between the ages of 8 and 26 with most of the ...

Q: Is there a cure for myoclonic epilepsy? A: Yes, juvenile myoclonic epilepsy (JME) can be treated with medications. With the appropriate drugs, the condition can be managed and may, in some cases, ...

What Is Juvenile Myoclonic Epilepsy (JME)? Also known as Janz syndrome, JME is a common generalised epilepsy disorder that typically begins in adolescence or early adulthood. It is characterised by ...

A 20-year-old woman presented to a specialist epilepsy center with seizures, myoclonus, ataxia, and impaired executive functions. She was born to unrelated parents, had febrile seizures in infancy, ...

Benign adult familial myoclonic epilepsy (BAFME), alternatively named familial adult myoclonic epilepsy 1/familial cortical myoclonic tremor with epilepsy 1 (FAME1/FCMTE1), is a hereditary epileptic ...

The hospital pharmacies dominated the segment during forecast period. Doctors and hospital pharmacists are an essential component of the segment because pharmacists assist patients with the disease ...

Fast, reliable and automatic assessment of the severity of myoclonic jerks from video footage is now possible, thanks to an algorithm using deep convolutional neural network architecture and ...

Research groups from the University of Helsinki, the LMU Munich and the University of Guelph have described in collaboration a novel myoclonic epilepsy in dogs and identified its genetic cause. The ...