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  • renal cortical adenoma
    ½ÅÇÇÁú¼±Á¾
  • renal cortical microcystic disease
    ½ÅÇÇÁú¹Ì¼¼³¶Á¾Áúȯ
  • renal cortical necrosis
    ½ÅÇÇÁú±«»ç(ãìù«òõ ÎÕÞÝ).
  • renal cortical necrosis
    ½ÅÇÇÁú±«»ç(ãìù«òõ ÎÕÞÝ)
  • subperiosteal cortical thickening
    °ñ¸·ÇÏ °ñÇÇÁúºñÈÄ(Í騝ù»Íéù«òõÝþý§).
  • subperiosteal cortical thickening
    °ñ¸·ÇϰñÇÇÁúºñÈÄ(Í騝ù»Íéù«òõÝþý§)
  • abdominal epilepsy
  • abortive epilepsy
    ºÎÀü°£Áú.
  • affect epilepsy
    Á¤µ¿¼º °£Áú(ï×ÔÑàõÊÖòð).
  • akinetic epilepsy
    ¹«µ¿¼º °£Áú(¡­ÊÖòð).
  • alcoholic epilepsy
    ¾ËÄڿüº °£Áú(¡­ÊÖòð).
  • arithmetical epilepsy
    »ê¼ú¼º °£Áú
  • autonomic epilepsy
    ÀÚÀ²½Å°æ°è °£Áú
  • benign partial epilepsy of childhood
    ¼Ò¾Æ±â ¾ç¼ººÎºÐ°£Áú
  • centrencephalic epilepsy
    Á߽ɳú¼º°£Áú(ñéãýÒààõÊÖòð).
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DCR dacryocystorhinostomy; data conversion receiver; direct cortical response
DCS decompression sickness; dense canalicular system; diffuse cortical sclerosis; dorsal column stimulat...
DME degenerative myoclonus epilepsy; dimethyl diester; dimethyl ether; diphasic meningoencephalitis; dir...
EAA electroacupuncture analgesia; Epilepsy Association of America; essential amino acid; excitatory amin...
EFA Epilepsy Foundation of America; essential fatty acid; extrafamily adoptee
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MERRF myoclonus epilepsy and ragged red fiber
CCT Combined cortical thickness
CCI Controlled cortical impact
C Cortical
CSD Cortical Spreading Depression
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somnambulic epilepsy Postictal automatism in which the patient walks or runs about exhibiting natural behaviour of which he or she has no subsequent remembrance.
(05 Mar 2000)
startle epilepsy A form of reflex epilepsy precipitated by sudden noises.
(05 Mar 2000)
nocturnal epilepsy An epilepsy syndrome characterised by nocturnal seizures only.
(05 Mar 2000)
supplementary motor area epilepsy A localization-related epilepsy syndrome in which seizures originate from the supplementary motor area of the mesial frontal lobe. Typical seizure semiology includes sudden bilateral tonic movements, vocalization, and preservation of consciousness. Attacks are often nocturnal.
(05 Mar 2000)
symptomatic epilepsy A group of epilepsy syndromes of diverse aetiologies with diffuse or multifocal cerebral involvement. Patients typically have a variety of generalised seizure types, including tonic, atonic, myoclonic, atypical absence, and generalised tonic-clonic seizures. Partial seizures may also occur. One classic syndrome is the Lennox-Gastaut syndrome.
Synonym: symptomatic epilepsy.
(05 Mar 2000)
diencephalic epilepsy Episodes of autonomic dysfunction presumably due to diencephalic irritation.
Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy.
(05 Mar 2000)
idiopathic epilepsy An epilepsy without evident cause; term often used to describe the genetic epilepsies.
Synonym: generalised tonic-clonic seizure.
(05 Mar 2000)
intractable epilepsy Epilepsy not adequately controlled by medication.
Synonym: pharmacoresistent epilepsy.
(05 Mar 2000)
occipital lobe epilepsy A localization-related epilepsy where seizures originate from the occipital lobe. Symptoms commonly include visual abnormalities during seizures.
(05 Mar 2000)
temporal lobe epilepsy Seizures with elaborate and multiple sensory, motor, and/or psychic components. A common feature is the clouding of consciousness and amnesia for the event. Some clinical manifestations may include more complex behaviours like burst of anger, emotional outbursts, fear or automatisms. The EEG often reveals spike discharges in the temporal lobe during sleep.
(27 Sep 1997)
early posttraumatic epilepsy Seizures beginning within one week after severe head injury.
(05 Mar 2000)
eating epilepsy Epileptic, often generalised, seizures provoked by eating; a type of reflex epilepsy.
(05 Mar 2000)
tonic epilepsy An attack in which the body is rigid.
(05 Mar 2000)
tornado epilepsy A type of focal epilepsy or partial seizure with an aura of severe vertigo and a feeling of being drawn up into space.
(05 Mar 2000)
epilepsy <disease, neurology> The paroxysmal transient disturbances of brain function that may be manifested as episodic impairment or loss of consciousness, abnormal motor phenomena, psychic or sensory disturbances or perturbation of the autonomic nervous system.
Symptoms are due to paroxysmal disturbance of the electrical activity of the brain. On the basis of origin, epilepsy is idiopathic (cryptogenic, essential, genetic) or symptomatic (acquired, organic). On the basis of clinical and electroencephalographic phenomenon, four subdivisions are recognised:
1. Grand mal epilepsy (major epilepsy, haut mal epilepsy) subgroups: generalised, focal (localised), jacksonian (rolandic)
2. Petit mal epilepsy
3. Psychomotor epilepsy (temporal lobe epilepsy, psychic, psychic equivalent or variant) subgroups: psychomotor proper (tonic with adversive or torsion movements or masticatory phenomena), automatic (with amnesia) and sensory (hallucinations or dream states or d‚j. Vu)
4. Autonomic epilepsy (diencephalic), with flushing, pallor, tachycardia, hypertension, perspiration or other visceral symptoms.
Synonym: epilepsia.
Origin: Gr. Epilepsia = seizure
(14 May 1997)
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