Epilepsy

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Related to Myoclonic epilepsy: myoclonic astatic epilepsy, juvenile myoclonic epilepsy, Myoclonic Epilepsy with Ragged Red Fibers

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 ?
The adverse events that result from Keppra(R) injection use for primary generalized tonic-clonic seizures in adults with idiopathic generalized epilepsy, myoclonic seizures in adults with juvenile myoclonic epilepsy and partial onset seizures in adults with epilepsy include all of those associated with Keppra(R) tablets and oral solution.
Absence, juvenile myoclonic epilepsy and familial neonatal seizures (seizures in the newborn) are three types of epilepsy that tend to run in families and are thought to have a genetic basis.
Juvenile myoclonic epilepsy is a common epilepsy syndrome that usually starts between the ages of 12 and 18 and accounts for about 10% of all cases of epilepsy(1).
Myoclonic seizures are the hallmark symptom of a juvenile myoclonic epilepsy (JME) diagnosis.
Key clinical point: Patients with juvenile myoclonic epilepsy generally have a long-term quality of life that is generally equal to or better than patients with childhood or juvenile absence epilepsy.
Used in severe myoclonic epilepsy in infancy (Dravet's syndrome)
Talking about juvenile myoclonic epilepsy (disorder characterised with abnormal movement of any part of the body when the patient wakes up in the morning) in Qatar, the official said there were many patients with the condition.
Juvenile myoclonic epilepsy (JME), also known as Janz syndrome, is a fairly common form of idiopathic generalised epilepsy, representing 10% of all epilepsy.
Dr John Jenkins from the University of London in 2001, found that when patients with myoclonic epilepsy were made to listen to classical music, the number of convulsions, and their severity, were significantly reduced.
I found I had juvenile myoclonic epilepsy, which typically starts with having a history of migraines, which I did, and then the sufferer starts collapsing in puberty, then having seizures.
New technology that permits the sequencing of 20,000 genes for less than $1,000 is leading to the rapid discovery of genes underlying rare forms of epilepsy, such as the identification of the GOSR2 gene responsible for progressive myoclonic epilepsy (Am.