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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
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Classification of myoclonus by clinical syndrome and etiology

Classification of myoclonus by clinical syndrome and etiology
  1. Physiologic myoclonus
  1. Sleep jerks (eg, hypnic jerks)
  1. Anxiety-induced
  1. Exercise-induced
  1. Hiccough (singultus)
  1. Benign infantile myoclonus with feeding
  1. Essential myoclonus (primary symptom, nonprogressive history)
  1. Hereditary (autosomal dominant)
  1. Sporadic
  1. Epileptic myoclonus (associated with a chronic seizure disorder or syndrome)
  1. Fragments of epilepsy
  1. Isolated epileptic myoclonic jerks
  1. Epilepsia partialis continua
  1. Idiopathic stimulus-sensitive myoclonus
  1. Photosensitive myoclonus
  1. Absences with a minor myoclonic component
  1. Epilepsy with myoclonic absences
  1. Childhood myoclonic epilepsy
  1. Infantile spasms (West syndrome)
  1. Severe myoclonic epilepsy of infancy (Dravet syndrome)
  1. Benign myoclonic epilepsy of infancy
  1. Lennox-Gastaut syndrome
  1. Myoclonic astatic epilepsy (Doose syndrome)
  1. Cryptogenic myoclonus epilepsy (Aicardi)
  1. Juvenile myoclonic epilepsy (Janz syndrome)
  1. Familial cortical myoclonic tremor with epilepsy
  1. Autosomal dominant cortical myoclonus and epilepsy
  1. Benign adult familial myoclonic epilepsy
  1. Cortical tremor
  1. Familial adult myoclonic epilepsy
  1. Familial cortical myoclonic tremor
  1. Familial cortical tremor with epilepsy
  1. Familial essential myoclonus and epilepsy
  1. Familial rhythmic cortical myoclonus (tremor) with epilepsy
  1. Familial benign myoclonus epilepsy of adult onset
  1. Heredofamilial tremor and epilepsy
  1. Symptomatic (secondary) myoclonus (not defined by occurrence of seizures)
  1. Progressive myoclonic epilepsy: Unverricht-Lundborg disease (Baltic myoclonus)
  1. Storage disease
  1. Lafora body disease
  1. GM2 gangliosidosis (late infantile, juvenile)
  1. Tay-Sachs disease
  1. Gaucher disease (noninfantile neuronopathic form)
  1. Krabbe leukodystrophy
  1. Neuronal ceroid lipofuscinosis
  1. Sialidosis (types 1 and 2)
  1. Spinocerebellar degenerations
  1. Progressive myoclonus ataxia (Ramsay-Hunt cerebellar syndrome)
  1. Friedreich ataxia
  1. Ataxia-telangiectasia
  1. Other spinocerebellar degenerations
  1. Basal ganglia degenerations
  1. Wilson disease
  1. Torsion dystonia
  1. Pantothenate kinase-associated neurodegeneration
  1. Progressive supranuclear palsy
  1. Huntington disease
  1. Parkinson disease
  1. Multiple system atrophy
  1. Corticobasal degeneration
  1. Dentatorubral pallidoluysian atrophy
  1. Dementias
  1. Creutzfeldt-Jakob disease
  1. Alzheimer disease
  1. Dementia with Lewy bodies
  1. Frontotemporal dementia
  1. Rett syndrome
  1. Diffuse infectious/postinfectious/inflammatory disorders
  1. Subacute sclerosing panencephalitis
  1. Encephalitis lethargica
  1. Arbovirus encephalitis
  1. Herpes simplex encephalitis
  1. Human T-lymphotropic virus I
  1. Human immunodeficiency virus (HIV)
  1. Postinfectious encephalitis
  1. Miscellaneous bacteria (Streptococcus, Clostridium, other)
  1. Malaria
  1. Syphilis
  1. Cryptococcus
  1. Lyme disease
  1. Paraneoplastic
  1. Progressive multifocal leukoencephalopathy
  1. Metabolic
  1. Hyperthyroidism
  1. Hepatic failure
  1. Renal failure
  1. Dialysis syndrome
  1. Hyponatremia
  1. Hypoglycemia
  1. Nonketotic hyperglycemia
  1. Multiple carboxylase deficiency
  1. Biotin deficiency
  1. Hypoxia
  1. Metabolic alkalosis
  1. Vitamin E deficiency
  1. Toxic and drug-induced syndromes
  1. Drugs
  1. Levodopa
  1. Psychiatric medications (eg, tricyclic antidepressants, selective serotonin reuptake inhibitors, monoamine oxidase inhibitors, lithium)
  1. Antibiotics (eg, penicillins, cephalosporins, quinolones)
  1. Narcotics
  1. Antiseizure medications (eg, gabapentin, lacosamide, lamotrigine, phenytoin, pregabalin, valproate)
  1. Anesthetics
  1. Contrast media
  1. Cardiac medications (eg, calcium channel blockers, antiarrhythmic agents)
  1. Drug withdrawal from certain agents (eg, sedatives)
  1. Toxins
  1. Bismuth
  1. Heavy metals
  1. Methyl bromide
  1. Dichlorodiphenyltrichloroethane (DDT)
  1. Physical encephalopathies (usually static)
  1. Posthypoxic (Lance-Adams)
  1. Posttraumatic
  1. Heat stroke
  1. Electric shock
  1. Decompression injury
  1. Focal nervous system damage
  1. Central nervous system
  1. Poststroke
  1. Postthalamotomy
  1. Tumor
  1. Trauma
  1. Infection
  1. Inflammation (eg, multiple sclerosis)
  1. Moebius syndrome
  1. Developmental
  1. Idiopathic
  1. Peripheral nervous system
  1. Trauma
  1. Hematoma
  1. Malabsorption
  1. Celiac disease
  1. Whipple disease
  1. Eosinophilia-myalgia syndrome
  1. Opsoclonus-myoclonus syndrome
  1. Idiopathic
  1. Paraneoplastic
  1. Infectious
  1. Other
  1. Exaggerated startle syndrome
  1. Hereditary
  1. Sporadic
  1. Hashimoto encephalopathy
  1. Other multiple system degenerations
  1. Action myoclonus-renal failure syndrome
  1. Mitochondrial disorders
  1. Allgrove syndrome
  1. DiGeorge syndrome
  1. Membranous lipodystrophy
  1. Primary progressive myoclonus of aging
  1. Unknown
  1. Familial
  1. Sporadic
Modified from: Marsden CD, Hallett M, Fahn S. The nosology and pathophysiology of myoclonus. In: Movement Disorders, Marsden CD, Fahn S (Eds), Butterworths, London 1982. p.196.
Graphic 78331 Version 10.0

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