| pupillary block glaucoma | Glaucoma secondary to failure of the aqueous humor to pass through the pupil to the anterior chamber. (05 Mar 2000) |
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| 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) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
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