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  • petit mal epilepsy
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  • running epilepsy
    ÁúÁÖ°£Áú
  • reflex epilepsy
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  • sensory epilepsy
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  • sleep-related epilepsy
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  • temporal lobe epilepsy
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  • tardy epilepsy
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  • photosensitive epilepsy
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  • post-apoplectic epilepsy
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  • post-stroke epilepsy
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  • post-traumatic epilepsy
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  • primary epilepsy
    ¿ø¹ß°£Áú, ÀÏÂ÷°£Áú
  • psychomotor epilepsy
    Á¤½Å¿îµ¿°£Áú
  • reflex epilepsy
    ¹Ý»ç°£Áú
  • retrocursive epilepsy
    ÈÄÅð°£Áú
  • running epilepsy
    ÁúÁÖ°£Áú
  • senile epilepsy
    ³ëÀΰ£Áú
  • sensory epilepsy
    °¨°¢°£Áú
  • sleep-related epilepsy
    ¼ö¸é°ü·Ã°£Áú
  • somnambulistic epilepsy
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  • tardy epilepsy
    Áß³âÀÌÈİ£Áú
  • verbomotor epilepsy
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  • gustatory epilepsy
    ¹Ì°¢¼º °£Áú.
  • hereditary epilepsy
    À¯Àü¼º °£Áú(¡­ÊÖòð).
  • hiernosus =epilepsy
    °£Áú(ÊÖòð).
  • hysterical epilepsy
    È÷½ºÅ׸®¼º °£Áú
  • idiopathic epilepsy
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  • juvenile myoclonic epilepsy
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  • laryngeal epilepsy
    Èĵμº Çö±â(¡­úßѨ).
  • latent epilepsy
    Àẹ°£Áú(íÖÜÑÊÖòð).
  • limbic epilepsy personality syndrome
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  • local epilepsy
    ±¹¼Ò°£Áú(¡­ÊÖòð).
  • major epilepsy
    ´ë°£Áú(ÓÞÊÖòð).
  • masked epilepsy
    °¡¸é°£Áú(Ê£ØüÊÖòð).
  • menstrual epilepsy
    ¿ù°æ¼º °£Áú(¡­ÊÖòð).
  • minor epilepsy
    ¼Ò°£Áú(á³ÊÖòð).
  • morpheic epilepsy
    ¼ö¸éÇü°£Áú(â²Øùû¡ ÊÖòð).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
OHR occupational health research; Office of Health Research
MERRF Syndrome Myoclonic Epilepsy & Ragged Red Fibers Syndrome
BCE basal cell epithelioma; benign childhood epilepsy; bubble chamber equipment
BFEC benign focal epilepsy of childhood
BOE benign occipital epilepsy
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
ILAE International League Against Epilepsy
JME Juvenile Myoclonic Epilepsy
JAE Juvenile absence epilepsy
MTLE Medial temporal lobe epilepsy
MERRF Myoclonic Epilepsy and Ragged Red Fibers
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
vasovagal epilepsy Episodes of autonomic dysfunction presumably due to diencephalic irritation.
Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy.
(05 Mar 2000)
generalised epilepsy A major category of epilepsy syndromes characterised by one or more types of generalised seizures.
(05 Mar 2000)
generalised tonic-clonic epilepsy tonic-clonic seizure
masked epilepsy A form of epilepsy characterised by a paroxysmal disturbance, such as headache or vomiting, associated with an epileptic electroencephalographic pattern.
(05 Mar 2000)
parietal lobe epilepsy A localization-related epilepsy where seizures originate within the parietal lobe. Seizure semiology may involve abnormalities of sensation.
(05 Mar 2000)
matutinal epilepsy A form of epilepsy which occurs on awakening.
(05 Mar 2000)
reflex epilepsy Seizures which are induced by peripheral stimulation; e.g., audiogenic, laryngeal, photogenic, or other stimulation.
Synonym: sensory precipitated epilepsy.
(05 Mar 2000)
partial epilepsy Epilepsy of various aetiologies characterised by focal seizures or secondarily generalised tonic-clonic seizures. Ictal symptoms are often related to the brain region where the seizure begins focally.
Synonym: cortical epilepsy, local epilepsy, partial epilepsy.
(05 Mar 2000)
visceral epilepsy Epilepsy, usually psychomotor, in which the attacks are initiated by visceral symptoms or sensations; most cases have their focus in the temporal lobe.
(05 Mar 2000)
pattern sensitive epilepsy A form of reflex epilepsy precipitated by viewing certain patterns.
(05 Mar 2000)
centrencephalic epilepsy An imprecise term referring to epilepsy characterised electroencephalographically by bilateral synchronous discharges, and clinically by absence or generalised tonic-clonic seizures.
(05 Mar 2000)
grand mal epilepsy Older term for epilepsy characterised by generalised tonic-clonic seizure.
(05 Mar 2000)
childhood absence epilepsy A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures.
See: absence.
Synonym: petit mal epilepsy, pyknolepsy.
(05 Mar 2000)
childhood epilepsy with occipital paroxysms A benign epilepsy syndrome characterised by frequent occipital spikes often activated by eye closure. It has a seizure semiology that includes visual manifestations; not always remitting later in life.
(05 Mar 2000)
petit mal epilepsy A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures.
See: absence.
Synonym: petit mal epilepsy, pyknolepsy.
(05 Mar 2000)
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