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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 11
  • Epilepsia Partialis Continua - »õâ A variant of epilepsy characterized by continuous focal jerking of a body part over a period of hours, days, or even years without spreading to other body regions. Contractions may be aggravated by movement and are reduced, but not abolished during sleep. ELECTROENCEPHALOGRAPHY demonstrates epileptiform (spike and wave) discharges over the hemisphere opposite to the affected limb in most instances. The repetitive movements may originate from the CEREBRAL CORTEX or from subcortical structures (e.g., BRAIN STEM; BASAL GANGLIA). This condition is associated with Russian Spring and Summer encephalitis (see ENCEPHALITIS, TICK BORNE); Rasmussen syndrome (see ENCEPHALITIS); MULTIPLE SCLEROSIS; DIABETES MELLITUS; BRAIN NEOPLASMS; and CEREBROVASCULAR DISORDERS. (From Brain, 1996 April;119(pt2):393-407; Epilepsia 1993;34;Suppl 1:S29-S36; and Adams et al., Principles of Neurology, 6th ed, p319)
    Synonyms : Chronic Progressive Epilepsia Partialis Continua, Epilepsia Partialis Continua, Chronic Progressive, Kojevnikov's Epilepsy, Kojewnikov's Epilepsy, Kojewnikow's Syndrome, Kozhevnikov's Syndrome, Kozhevnikow Syndrome, Progressive Variant, Epilepsy, Kojevnikov's
  • 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
  • Epilepsies, Partial - »õâ Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317)
    Synonyms : Amygdalo-Hippocampal Epilepsy, Benign Focal Epilepsy, Childhood, Benign Occipital Epilepsy, Childhood, Childhood Benign Focal Epilepsy, Childhood Benign Occipital Epilepsy, Epilepsy, Localization-Related, Epilepsy, Partial, Occipital Lobe Epilepsy
  • Epilepsy - »õâ A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)
    Synonyms : Epilepsy, Cryptogenic, Seizures, Epileptic, Single Seizure, Auras, Cryptogenic Epilepsies, Cryptogenic Epilepsy, Epilepsies, Epilepsies, Cryptogenic, Epilepsy, Awakening, Epileptic Seizure, Seizure Disorders, Seizure, Epileptic, Seizure, Single, Seizures, Single
  • Epilepsy, Absence - »õâ A childhood seizure disorder characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736)
    Synonyms : Absence Seizure Disorder, Atonic Absence Seizures, Childhood Absence Epilepsy, Epilepsy, Absence, Atypical, Epilepsy, Petit Mal, Juvenile Absence Epilepsy, Petit Mal Convulsion, Pykno-Epilepsy, Seizure Disorder, Absence, Absence Epilepsies, Childhood
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 11
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