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EPILEPSY, med. jur. A disease of the brain, which occurs in paroxysms, with uncertain intervals between them.
     2. These paroxysms are characterized by the loss of sensation, and convulsive motions of the muscles. When long continued and violent, this disease is very apt to end in dementia. (q.v.) It gradually destroys the memory, and impairs the intellect, and is one of the causes of an unsound mind. 8 Ves. 87. Vide Dig. 50, 16, 123; Id. 21, 1, 4, 5.

References in periodicals archive ?
2 frequency (1-6) (0-8) (per month) (per year) MTLEHS: Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis, JME: Juvenile Myoclonic Epilepsy Table 3.
Major finding: Adult juvenile myoclonic epilepsy patients without comorbid psychiatric conditions had quality of life scores that were similar, or higher, than in absence epilepsy controls (P = .
1 Janz described Juvenile Myoclonic Epilepsy (JME) for the first time in 1957.
I am personally following at least 25 patients with juvenile myoclonic epilepsy aged between 7 and 16 years.
juvenile myoclonic epilepsy, many structural-metabolic (symptomatic) focal epilepsies: relapse occurs with attempted drug withdrawal, treatment usually lifelong
Epilepsies with onset in adolescence included juvenile absence epilepsy, juvenile myoclonic epilepsy, generalized tonic-clonic seizures on awakening, photosensitive epilepsy, mesial temporal lobe epilepsy, progressive myoclonic epilepsy and other partial or generalized epilepsies.
We invited caregivers of 50 patients with temporal lobe epilepsy (TLE) related to mesial temporal sclerosis and caregivers of 50 patients with juvenile myoclonic epilepsy (JME) to participate.
These include benign rolandic epilepsy, juvenile myoclonic epilepsy and temporal lobe epilepsy.
The FDA granted an additional indication for Keppra (levetiracetam), manufactured by UCB (Brussels, Belgium), as an adjunctive therapy in the treatment of myoclonic seizures in adults and adolescents 12 years of age and older with juvenile myoclonic epilepsy.
Her family eventually persuaded her to go to hospital where she was diagnosed with juvenile myoclonic epilepsy.

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