| AION | Anterior Ischemic Optic Neuropathy |
|---|---|
| AION | anterior ischemic optic neuropathy |
| AOT | accessory optic tract; Anderson Olsson table; anodal opening tetanus; Association of Occupational Th... |
| BOR | basal optic root; before time of operation; bowels open regularly; branchio-oto-renal [syndrome] |
| COT | colony overlay test; content of thought; contralateral optic tectum; critical off-time |
| suboccipital neuritis | See: posttraumatic neck syndrome. (05 Mar 2000) |
|---|---|
| descending neuritis | Inflammation progressing downward along a nerve trunk in a direction toward the periphery. (05 Mar 2000) |
| interstitial neuritis | Inflammation of the connective tissue framework of a nerve. Synonym: Eichhorst's neuritis. (05 Mar 2000) |
| intraocular neuritis | Inflammation of the retinal portion of the optic nerve. (05 Mar 2000) |
| occipital neuritis | See: posttraumatic neck syndrome. (05 Mar 2000) |
| Eichhorst's neuritis | Inflammation of the connective tissue framework of a nerve. Synonym: Eichhorst's neuritis. (05 Mar 2000) |
| toxic neuritis | Neuritis caused by an endogenous or exogenous toxin. (05 Mar 2000) |
| endemic neuritis | <disease> An endemic form of polyneuritis (nerve inflammation), due to an unbalanced diet, with a deficiency of vitamin B1(thiamin). Common in those who chronically abuse alcohol. (11 Jan 1998) |
| traumatic neuritis | Nerve lesion following an injury. (05 Mar 2000) |
| fallopian neuritis | Paralysis of the facial muscles, usually unilateral, due to either a lesion involving the nucleus or the facial nerve peripheral to the nucleus (peripheral facial paralysis) or a supranuclear lesion in the cerebrum or upper brainstem (central facial paralysis). With latter, facial weakness is usually partial and the upper portion of the face is relatively spared, due to bilateral cortical connections. (12 Dec 1998) |
| Leyden's neuritis | Fatty degeneration of the fibres of the affected nerve. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |