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 ...

Gaucher disease, the inherited deficiency of lysosomal glucocerebrosidase, presents with a wide spectrum of manifestations. Although Gaucher disease has been divided into three clinical types, ...

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 ...

Sleep myoclonus is involuntary, nonrhythmic muscle twitching that occurs either as a person falls asleep or during sleep. The movements include hiccups, starts, and jerks. Sleep myoclonus is not a ...

The severity of epilepsy-related muscle pricking symptoms can be reliably estimated with artificial intelligence, according to a recent study. An artificial intelligence-based tool was used to analyze ...

A new study shows that wearable sensor technology can be used to reliably assess the occurrence of myoclonic jerks in patients with epilepsy also in the home environment. A new study by the University ...

Research groups have described in collaboration a novel myoclonic epilepsy in dogs and identified its genetic cause. The study reveals a novel candidate gene for human myoclonic epilepsies, one of the ...

Levetiracetam 100mg/mL; grape flavor; dye-free. Swallow tabs whole. Partial onset: ≥16yrs: initially 500mg twice daily. May increase at 2-week intervals in increments of 1g/day; max 3g/day. Myoclonic: ...