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MERRF Syndrome Myoclonic Epilepsy & Ragged Red Fibers Syndrome
MTA malignant teratoma, anaplastic; medical technical assistant; medical technology assessment; metatars...
SME severe myoclonic epilepsy
SMEI severe myoclonic epilepsy of infancy
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IGEs idiopathic generalised epilepsies
JME Juvenile Myoclonic Epilepsy
MERRF Myoclonic Epilepsy and Ragged Red Fibers
MERRF Myoclonic epilepsy with ragged-red fibers
PME Progressive myoclonic epilepsy
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myoclonic Showing myoclonus.
(05 Mar 2000)
myoclonic astatic epilepsy A petit mal variant characterised by atonic (drop attacks) and tonic or tonic-clonic attacks in neurologically disabled (hemiplegic, ataxic, etc.) children with mental retardation; characterised in EEG by 2/sec spike and wave discharges; usually progresses in spite of medication.
(05 Mar 2000)
myoclonic seizure Seizure associated with single or repetitive myoclonic jerks.
(05 Mar 2000)
epilepsy, myoclonic A progressive encephalopathy characterised by myoclonic jerks (single or repetitive muscle contractions involving one body part or the entire body), mental retardation, and ataxia. The disease, an autosomal recessive form of epilepsy, occurs usually at puberty. The most significant pathological findings are lafora's inclusion bodies, which contain mucopolysaccharides.
(12 Dec 1998)
epilepsy with myoclonic absences A form of generalised epilepsy characterised by absence seizures, severe bilateral rhythmic clonic jerks often associated with tonic contraction, and an EEG 3 Hz spike and wave pattern. Age of onset is usually around seven years and males are more often affected.
(05 Mar 2000)
juvenile myoclonic epilepsy An epilepsy syndrome typically beginning in early adolescence, and characterised by early morning myoclonic jerks that may progress into a generalised tonic-clonic seizure. A genetic disorder: some families have had gene linkage to chromosome-6. The EEG is characterised by generalised polyspike and wave discharges at 4-6 Hz.
(05 Mar 2000)
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  • Epilepsies, Myoclonic - »õâ A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic (i.e., occurring secondary to known disease processes such as infections, hypoxic-ischemic injuries, trauma, etc.).
    Synonyms : Benign Infantile Myoclonic Epilepsy, Cryptogenic Myoclonic Epilepsy, Early Childhood Epilepsy, Myoclonic, Early Childhood, Myoclonic Epilepsy, Encephalopathy, Myoclonic, Epilepsy, Early Childhood, Myoclonic, Epilepsy, Myoclonic, Early Childhood
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