myoclonic


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my·oc·lo·nus

 (mī-ŏk′lə-nəs)
n.
A sudden irregular twitching of muscles or parts of muscles, occurring in various brain disorders.

my′o·clon′ic (mī′ə-klŏn′ĭk) adj.

myoclonic

(ˌmaɪəˈklɒnɪk)
adj
(Medicine) of or relating to myoclonus
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References in periodicals archive ?
DS, also known as severe myoclonic epilepsy in infancy, is an orphan disease considered one of the most intractable forms of epilepsy, with first seizures occurring during the first year of life.
Ysgol Maes Garmon pupil Katie Potter, 13, from Northop, Flintshire, was diagnosed with juvenile myoclonic epilepsy around April 2018.
The literature has described clozapine-induced generalized tonic-clonic, myoclonic, simple and complex partial, and absence seizures.
A few months later, I received a diagnosis - juvenile myoclonic epilepsy (JME).
Conclusion: Majority of patients had symptomatic infantile spasms and generalized tonic clonic along with myoclonic jerks were predominant seizure types.
"The Tonic Clonic seizures and myoclonic seizures are uncontrollable and relentless, meaning that no emergency intervention is working to stop the continuous seizures.
Background: Treatment of myoclonic seizures in myoclonic epilepsy with ragged-red fibers (MERRFs) has been empirical and ineffective.
Later, other types of seizures typically arise, including myoclonic seizures (involuntary muscle spasms).
Dravet syndrome, also known as severe myoclonic epilepsy in infancy (SMEI), is a catastrophic early onset epileptic syndrome that is thought to affect approximately 2,000 to 8,000 patients in the US.