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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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JME Juvenile Myoclonic Epilepsy
MERRF Myoclonic Epilepsy and Ragged Red Fibers
MERRF Myoclonic epilepsy with ragged-red fibers
PME Progressive myoclonic epilepsy
SMEI Severe myoclonic epilepsy in infancy
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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)
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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)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 3 ÆäÀÌÁö: 1
  • Myoclonic Cerebellar Dyssynergia - »õâ A condition marked by progressive CEREBELLAR ATAXIA combined with MYOCLONUS usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal SEIZURES, spasticity, and DYSKINESIAS. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the CEREBELLUM are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1)
    Synonyms : Dentate Cerebellar Ataxia, Dentate Nucleus Syndrome, Ramsay Hunt, Dyssynergia Cerebellaris Progressiva, Ramsay Hunt Dentate Syndrome, Ataxia, Dentate Cerebellar, Ataxias, Dentate Cerebellar, Atrophies, Dentate Cerebellar, Atrophy, Dentate Cerebellar
  • Myoclonic Epilepsies, Progressive - »õâ A heterogeneous group of primarily familial disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME.
    Synonyms : Atypical Inclusion-Body Disease, Familial Progressive Myoclonic Epilepsy, Progressive Myoclonic Epilepsy, Progressive Myoclonus Epilepsies, Action Myoclonus Renal Failure Syndrome, Atrophies, Dentatorubral-Pallidoluysian, Atypical Inclusion Body Disease
  • Myoclonic Epilepsy, Juvenile - »õâ A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323)
    Synonyms : Impulsive Petit Mal Epilepsy, JME (Juvenile Myoclonic Epilepsy), Janz Impulsive Petit Mal, Janz Juvenile Myoclonic Epilepsy, Juvenile Myoclonic Epilepsy of Janz, Myoclonic Epilepsy, Adolescent, Petit Mal, Impulsive, Janz, Adolescent Myoclonic Epilepsies
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myoclonic dementia dementia myoclo
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
myoclonic encephalopathy 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_hl_dorlands.jspz...
myoclonic seizure A specific type of seizure in which the person may jerk and twitch but will not lose consciousness.
Ãâó: www.ehealthmd.com/library/epilepsy/EPI_glossary.ht...
myoclonic A type of muscle contraction.
Ãâó: www.bdid.com/termsm.htm
myoclonic Pertaining to myoclonus or irregular, involuntary, shock-like contractions or spasms of a muscle or muscle group.
Ãâó: www.dbs-stn.org/glossary2.asp
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