| EAA | electroacupuncture analgesia; Epilepsy Association of America; essential amino acid; excitatory amin... |
|---|---|
| EFA | Epilepsy Foundation of America; essential fatty acid; extrafamily adoptee |
| EPI | echo planar imaging; electronic portal imaging; Emotion Profile Index; epilepsy; epinephrine; epithe... |
| epil | epilepsy, epileptic |
| GE | gastric empyting; gastroemotional; gastroenteritis; gastroenterology; gastroenterostomy; gastroesoph... |
| secondary generalised 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) |
|---|---|
| sensory epilepsy | Focal epilepsy initiated by a somatosensory phenomenon. (05 Mar 2000) |
| sensory precipitated epilepsy | Seizures which are induced by peripheral stimulation; e.g., audiogenic, laryngeal, photogenic, or other stimulation. Synonym: sensory precipitated epilepsy. (05 Mar 2000) |
| sleep epilepsy | Incorrect term for narcolepsy. (05 Mar 2000) |
| 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) |