| MERRF Syndrome | Myoclonic Epilepsy & Ragged Red Fibers Syndrome |
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| MTA | malignant teratoma, anaplastic; medical technical assistant; medical technology assessment; metatars... |
| SME | severe myoclonic epilepsy |
| SMEI | severe myoclonic epilepsy of infancy |
| JME | Juvenile Myoclonic Epilepsy |
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| MERRF | Myoclonic Epilepsy and Ragged Red Fibers |
| MERRF | Myoclonic epilepsy with ragged-red fibers |
| PME | Progressive myoclonic epilepsy |
| SMEI | Severe myoclonic epilepsy in infancy |
| myoclonic | Showing myoclonus. (05 Mar 2000) |
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| 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) |
| myoclonic e. |
any form of epilepsy accompanied by myoclonus, such as juvenile myoclonic e., Baltic myoclonic e., and Lafora's myoclonic e. See also progressive familial myoclonic e.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| myoclonic e. of childhood |
a neurologic disorder of unknown etiology with onset between ages one and three, characterized by myoclonus of trunk and limbs and by opsoclonus, with ataxia of gait and intention tremor; some cases have been associated with occult neuroblastoma. Called also Kinsbourne syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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