| ¿µ¹® | retinal detachment | ÇÑ±Û | ¸Á¸· ¹Ú¸® |
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| ¼³¸í | Ä«¸Þ¶ó¿¡ ÀÖ¾î¼ Çʸ§¿¡ ÇØ´çÇÏ´Â ´«ÀÇ ¸Á¸·Àº Å©°Ô µÎ °³ÀÇ ÃþÀ¸·Î ³ª´ ¼ö°¡ ÀÖ´Ù. ¾ÈÂÊ¿¡ ÀÖ´Â ½ÇÁ¦ÀÇ ºûÀ» °¨ÁöÇÏ´Â °¨°¢Ãþ°ú ¹Ù±ùÂÊÀÇ ¿ÜºÎÀÇ ºûÀ» Â÷´ÜÇÏ´Â »ö¼Ò»óÇÇÃþÀÌ ±×°ÍÀε¥ ±× »çÀÌ¿¡´Â ÀáÀçÀûÀÎ °ø°£ÀÌ ÀÖ¾î¼ ¶³¾îÁö±â°¡ ½±´Ù. ÀÌ »çÀ̰¡ ¶³¾îÁö¸é ¸Á¸·ÀÇ °¨°¢ÃþÀÌ ¸Á¸·ÀÇ »ö¼Ò»óÇÇÃþ°ú ºÐ¸®µÇ´Âµ¥ À̰ÍÀ» ¸Á¸·¹Ú¸®¶ó°í ÇÑ´Ù. ÀÌ ¸Á¸·ÀÇ ¹Ú¸®¿¡´Â ¿©·¯ °¡Áö ¿øÀÎÀÌ ÀÖÁö¸¸ °¨°¢ÃþÀÇ ¸Á¸·¿¡ ÀÛÀº ±¸¸ÛÀÎ ¿°ø(break)¿¡ ÀÇÇØ¼ ±×°÷À¸·Î ´«¼ÓÀ» ä¿ì°í ÀÖ´Â ¾×ü°¡ Èê·¯ µé¾î°¡¼ »ý±â´Â ¸Á¸·ÀÇ ¹Ú¸®¸¦ ¿°ø¼º ¸Á¸·¹Ú¸®(rhegmatogenous retinal detachment)¶ó Çϰí, ¾È±¸ÀÇ º´ÅÍ¿¡ ÀÇÇØ¼ ¾È±¸³»¿¡ ¼¶À¯Á¶Á÷ÀÌ »ý±â°í ±×°ÍÀÌ ¸Á¸·ÀÇ °¨°¢ÃþÀ» Àâ¾Æ ²ø¾î¼ ¸Á¸·ÀÌ ¹Ú¸®µÇ´Â °ßÀμº ¸Á¸·¹Ú¸®(traction retinal detachment) ¹× ¸Á¸·ÀÇ 2°³ÀÇ Ãþ¿¡ »ïÃâ¾×ÀÌ ±«¾î¼ »ý±â´Â »ïÃ⼺ ¸Á¸·¹Ú¸®(exudative retinal detachment) µî ¿°ø¿¡ ÀÇÇØ¼ »ý±â´Â ¸Á¸·¹Ú¸®°¡ ¾Æ´Ñ °ÍÀ» ºñ¿°ø¼º ¸Á¸·¹Ú¸®(nonrhegmatogenous retinal detachment)¶ó°í ¸»ÇÑ´Ù. |
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| ¿µ¹® | atrophy | ÇÑ±Û | À§Ãà(Áõ) |
|---|---|---|---|
| ¼³¸í | Á¶Á÷À̳ª ¼¼Æ÷ ȤÀº ±â°üÀÇ Å©±â°¡ ¿ø·¡ÀÇ Å©±â¿¡ ºñÇÏ¿© ÁÙ¾îµå´Â °ÍÀ» ÀÏÄ´ ¸». óÀ½ºÎÅÍ Å©±â°¡ ÀÛÀº ¹«Çü¼º/Çü¼ºÀúÇÏÁõ(aplasia/hypoplasia)¿Í ±¸º°µÈ´Ù. |
||
| RD | radial deviation; radiology department; rate difference; Raynaud disease; reaction of degeneration; ... |
|---|---|
| PRP | 1) Progressive Rubella Panencephalitis 2) Platelet Rich Plasma &... |
| PRE | photoreacting enzyme; physician's report of examination; pigmented retinal epithelium; preplacement ... |
| PMA | index of prevalence and severity of gingivitis, where P = papillary gingiva, M = marginal gingiva, a... |
| PPMA | progressive postmyelitis muscular atrophy |
| PRA | Progressive retinal atrophy |
|---|---|
| PMA | progressive muscular atrophy |
| CA | Cerebellar atrophy |
| CA | Cerebral atrophy |
| DRPLA | Dentato-rubral and pallido-luysian atrophy |
| progressive choroidal atrophy | An x chromosome-linked abnormality characterised by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness. (12 Dec 1998) |
|---|---|
| progressive circumscribed cerebral atrophy | Circumscribed atrophy of the cerebral cortex. Synonym: lobar sclerosis, progressive circumscribed cerebral atrophy. (05 Mar 2000) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| progressive muscular atrophy | A serious neurologic disease that results from the progressive degeneration of the motor neurons. (27 Sep 1997) |
| progressive spinal muscular atrophy | One of the subgroups of motor neuron disease; a progressive degenerative disorder of the motor neurons of the spinal cord, manifested as progressive, often symmetrical, weakness and wasting, typically beginning in the distal portions of the limbs, particularly in the upper extremities, and spreading proximally; fasciculation potentials are often present, but evidence of corticospinal tract disease (e.g., increased deep tendon reflexes, Babinski sign) is not. (05 Mar 2000) |
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (05 Mar 2000) |
| all-trans-retinal | The orange retinaldehyde resulting from the action of light on the rhodopsin of the retina, which converts the 11-cis-retinal component of the rhodopsin to all-trans-retinal plus opsin. Synonym: trans-retinal, visual yellow. (05 Mar 2000) |
| blood-retinal barrier | Specialised nonfenestrated tightly-joined endothelial cells that form a transport barrier for certain substances between the retinal capillaries and the retinal tissue. (12 Dec 1998) |
| central retinal artery occlusion | <ophthalmology> The sudden blockage of the retinal artery with a blood clot that commonly leads to a painless but irreversible blindness in that eye. (12 Jan 1998) |
| central retinal fovea | A depression in the centre of the macula retinae containing only cones and lacking blood vessels. Synonym: fovea centralis retinae, central pit. (05 Mar 2000) |
| central retinal vein occlusion | <ophthalmology> The sudden blockage of the retinal vein with blood clot that commonly leads to a painless irreversible blindness in that eye. (12 Jan 1998) |
| retinal | 1. <anatomy> Pertaining to the retina. 2. <biochemistry> The aldehyde of retinol, derived by the oxidative enzymatic splitting of absorbed dietary carotene and having vitamin A activity. In the retina, retinal combines with opsins to form visual pigments. One isomer, 11 cis retinal combines with opsin in the rods (scotopsin) to form rhodopsin or visual purple. Another, all trans retinal (trans r.), visual yellow, xanthopsin) results from the bleaching of rhodopsin by light, in which the 11 cis form is converted to the all trans form. Retinal also combines with opsins in the cones (photopsins) to form the three pigments responsible for colour vision. (18 Nov 1997) |
| retinal adaptation | Adjustment to degree of illumination. (05 Mar 2000) |
| retinal anlage tumour | A benign neoplasm of neuroectodermal origin that most often involves the anterior maxilla of infants in the first year of life. It presents clinically as a rapidly growing blue-black lesion producing a destructive radiolucency; histologically, it is characterised by small round undifferentiated tumour cells interspersed with larger polyhedral melanin-producing cells arranged in an alveolar configuration. Synonym: melanoameloblastoma, pigmented ameloblastoma, pigmented epulis, progonoma of jaw, retinal anlage tumour. (05 Mar 2000) |
| progressive retinal atrophy |
degeneration of the retinal vision cells which progresses to blindness. (info)
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