myoclonic


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my·o·clon·ic

(mī'ō-klon'ik),
Showing myoclonus.

my·o·clon·ic

(mī'ō-klon'ik)
Showing myoclonus.
References in periodicals archive ?
The most common type of epileptic spasm was generalized tonic clonic along with myoclonic jerks (38.7%) followed by flexor spasms (30.5%) and mixed type (28%).
Seizures, especially myoclonic seizures, are a common clinical feature of MERRF.[3] Until now, the treatment of myoclonic seizures in MERRF has been empirical, ineffective, and different from the treatments of other causes of myoclonic seizures.
(4) Clinical features Current study (2016) Sex Male Female Age of onset 1.5 years 8 months Perinatal history Unremarkable Unremarkable Family history Negative Positive Inheritance Autosomal recessive Autosomal recessive Seizures Absence, Atonic to Myoclonic seizures GTCS evolving to tonic and GTCS EEG Focal and Lennox-Gastaut generalized spike pattern waves Paroxysmal nonkinesigenic + - d yskinesia MRI Cerebellar and spinal Cerebellar atrophy tract atrophy KCNMA1 c.1372C>T c.2026dupT mutation (homozygous) (homozygous) Protein p.Arg458Ter p.(Try676Leufs*7) Inheritance Autosomal recessive Autosomal recessive Tabarki et al.
If a child in the family develops prodromal symptoms of complications such as flaccid paralysis, limb weakness, drowsiness, disturbed consciousness, inactivity, myoclonic jerk, continuous vomiting, tachypnea, and tachycardia, please ensure the child receive medical assistance at a large hospital as soon as possible, the agency said.
He had consulted 4 neurologists who had diagnosed him as having myoclonic epilepsy despite video electroencephalogram (EEG) and magnetic resonance imaging of the brain being found to be within normal limits.
demonstrated increased FC between the motor cortex and SMA based on cognitive task analysis in JME patients [18, 19], which hinted that cognitive activity triggered the myoclonic jerks [20].
It was previously known as Severe Myoclonic Epilepsy of Infancy, and affects one out of 15,700 individuals, 80 percent of whom have a mutation in their SCN1A gene, according to (https://www.dravetfoundation.org/what-is-dravet-syndrome/) Dravet Syndrome Foundation . 
Generalized seizures (58%) 58/100 were most common followed by (32%) 32/100 focal seizures, (4%) 4/100 absence, (4%) 4/100 unclassified, (1%) 1/100 myoclonic seizures and (1%) 1/100 infantile spasm (table-I).
Generalized myoclonic tremor in all extremities was also noted on examination.
Myoclonic syndrome is brief, sudden, results in muscle contractions of the whole body or some body parts.