| secondary glaucoma | Glaucoma occurring as a sequel of preexisting ocular disease or injury. (05 Mar 2000) |
|---|---|
| pupillary block glaucoma | Glaucoma secondary to failure of the aqueous humor to pass through the pupil to the anterior chamber. (05 Mar 2000) |
| hypersecretion glaucoma | Glaucoma caused by excessive formation of the aqueous humor. (05 Mar 2000) |
| simple glaucoma | <ophthalmology> A disorder which is characterised by increased pressure within the eyeball. This occurs secondary to the chronic blockage of normal fluid circulation within the eye. Increased pressure within the eye can cause damage to the optic nerve and eventual blindness. Glaucoma is the leading cause of blindness. Symptoms include decreased vision, halos around lights (worse at night) and mild chronic headaches. Treatment is generally with beta-blocker eyedrops. Synonym: chronic glaucoma, compensated glaucoma, simple glaucoma, glaucoma simplex. (22 Sep 2002) |
| narrow-angle glaucoma | angle-closure glaucoma |
| neovascular glaucoma | Glaucoma occurring in rubeosis iridis. (05 Mar 2000) |
| Donders' glaucoma | An obsolete eponym for open-angle glaucoma. (05 Mar 2000) |
| open-angle glaucoma | <ophthalmology> A disorder which is characterised by increased pressure within the eyeball. This occurs secondary to the chronic blockage of normal fluid circulation within the eye. Increased pressure within the eye can cause damage to the optic nerve and eventual blindness. Glaucoma is the leading cause of blindness. Symptoms include decreased vision, halos around lights (worse at night) and mild chronic headaches. Treatment is generally with beta-blocker eyedrops. Synonym: chronic glaucoma, compensated glaucoma, simple glaucoma, glaucoma simplex. (22 Sep 2002) |
| eyes, glaucoma | Disease (there is more than one type) characterised by increased pressure within the eye. Glaucoma can lead to blindness. Glaucoma is five times more likely to occur in Blacks than in Whites. Early detection of glaucoma is essential to the preservation of vision. Glaucoma can be treated with medications, laser or traditional surgery. (12 Dec 1998) |
| low tension glaucoma | Optic nerve atrophy and excavation with typical field defects of glaucoma but without abnormal increase in intraocular pressure. (05 Mar 2000) |
| arthritis, juvenile rheumatoid | Rheumatoid arthritis of children occurring in three major subtypes defined by the symptoms present during the first six months following onset: systemic-onset (still's disease, juvenile-onset) polyarticular-onset, and pauciarticular-onset. Adult-onset cases of still's disease (still's disease, adult-onset) are also known. Only one subtype of juvenile rheumatoid arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. (12 Dec 1998) |
| benign juvenile melanoma | A benign, slightly pigmented or red superficial small skin tumour composed of spindle-shaped, epithelioid, and multinucleated cells that may appear atypical; most common in children, but also appearing in adults. Synonym: benign juvenile melanoma, epithelioid cell nevus, spindle cell nevus. (05 Mar 2000) |
| rheumatoid arthritis, systemic-onset juvenile | Also known as systemic-onset juvenile chronic arthritis. Still's disease presents with systemic (bodywide) illness including high intermittent fever, a salmon-coloured skin rash, swollen lymph glands, enlargement of the liver and spleen, and inflammation of the lungs (pleuritis) and around the heart (pericarditis). The arthritis may not be immediately apparent but it does appear and may persist after the systemic symptoms are gone. (12 Dec 1998) |
| periodontitis, juvenile | Localised periodontitis in teenagers and young adults. The onset is during the circumpubertal period but the diagnosis can be made beyond puberty. Lesions are confined predominantly to the first permanent molars or incisors and the distribution of lesions is usually symmetrical. The gingiva may appear normal. The lesions are highly active immediately following puberty but later destruction may slow or cease spontaneously. The disease is four times more prevalent in females than males and more prevalent in african americans than in other races or ethnic groups. (12 Dec 1998) |
| xanthogranuloma, juvenile | Benign disorder of infants and children characterised by multiple nodules with lipid-laden, non-langerhans-cell histiocytes. (12 Dec 1998) |