| TLE | Temporal Lobe Epilepsy; 측두엽 간질 = Psychomotor Epilepsy; 정신 운동 간질 = Tem... |
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| AAO | American Academy of Osteopathy; American Academy of Ophthalmology; American Academy of Optometry; Am... |
| ACA | abnormal coronary artery; acrodermatitis chronica atrophicans; acute cerebellar ataxia; adenocarcino... |
| ACS | acrocallosal syndrome; acrocephalosyndactyly; acute chest syndrome; acute confusional state; Alcon C... |
| AOA | American Osteopathic Association; Administration on Aging; Alpha Omega Alpha Honor Society; American... |
| haemorrhagic fever, american | Diseases caused by american haemorrhagic fever viruses (tacaribe complex viruses). (12 Dec 1998) |
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| south american blastomycosis | A chronic fungal infection caused by Paracoccidioides brasiliensis, characterised by primary pulmonary lesions with dissemination to many visceral organs. Common findings include ulcerative granuloma lesions to the buccal mucosa (inner lining of the cheek) and nasal mucosa that extend to the surrounding skin. Generalised lymphangitis is also typical. More commonly seen in South America and the tropics. (27 Sep 1997) |
| South American trypanosomiasis | Trypanosomiasis caused by Trypanosoma (or Schizotrypanum) cruzi and transmitted by certain species of reduviid (triatomine) bugs. In its acute form, it is seen most frequently in young children, with swelling of the skin at the site of entry, most often the face, and regional lymph node enlargement; in its chronic form it can assume several aspects, commonly cardiomyopathy, but megacolon and megaesophagus also occur; natural reservoirs include dogs, armadillos, rodents, and other domestic, domiciliated, and wild mammals. Synonym: Chagas' disease, Chagas-Cruz disease, Cruz trypanosomiasis. (05 Mar 2000) |
| North American blastomycosis | A fungal infection caused by Blastomyces dermatitidis. This rare fungal infection may produce inflammatory lesion of the skin or lungs or present as a disseminated disease to the skin, lungs, bones, liver, spleen and central nervous system. Uncommon unless patient is immunocompromised (AIDS). (27 Sep 1997) |
| indians, central american | An ethnic group belonging to the mongoloid racial stock in central america. This does not include mexican indians. (12 Dec 1998) |
| indians, north american | An ethnic group belonging to the mongoloid racial stock in north america. (12 Dec 1998) |
| indians, south american | An ethnic group belonging to the mongoloid racial stock in south america. (12 Dec 1998) |
| oil of American wormseed | Volatile oil from the fresh above ground part of the flower, American wormseed, Chenopodium ambrosioides, or C. Anthelminticum. Used as an anthelmintic. Synonym: oil of American wormseed. (05 Mar 2000) |
| French-American-British classification | <haematology> The classification of acute myeloid leukaemia on the basis of bone marrow and peripheral blood features. M0: Acute myeloid leukaemia with minimal evidence of myeloid differentiation. M1: Acute myeloblastic leukaemia. M2: Acute myeloblastic leukaemia with differentiation. M3: Acute promyelocytic leukaemia. M4: Acute myelomonocytic leukaemia. M5: Acute monocytic leukaemia. M6: Acute erythroleukaemia. M7: Acute megakaryocytic leukaemia. Acronym: FAB (07 Apr 1998) |
| anosognosic epilepsy | Epilepsy characterised by attacks of which the person is unaware. Synonym: anosognosic seizures. (05 Mar 2000) |
| automatic epilepsy | <neurology> 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. (02 Jan 1998) |
| autonomic epilepsy | Episodes of autonomic dysfunction presumably due to diencephalic irritation. Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy. (05 Mar 2000) |
| benign childhood epilepsy with centrotemporal spikes | A specific epilepsy syndrome beginning in childhood and remitting in adolescence, characterised by nocturnal simple partial motor seizures or generalised tonic-clonic seizures. EEG shows centrotemporal spikes that are activated by sleep and an otherwise normal EEG background. (05 Mar 2000) |
| major epilepsy | tonic-clonic seizure |
| vasomotor epilepsy | Episodes of autonomic dysfunction presumably due to diencephalic irritation. Synonym: diencephalic epilepsy, vasomotor epilepsy, vasovagal epilepsy. (05 Mar 2000) |