| 영문 | cataract | 한글 | 백내장 |
|---|---|---|---|
| 설명 | 눈에서 카메라의 렌즈에 해당하는 부분인 수정체(lens)가 혼탁하게 변해서 시력의 장애가 생기는 것을 말한다. |
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| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
|---|---|
| MDPK | myotonic dystrophy protein kinase |
| MMD | mass median diameter; minimum morbidostatic dose; moyamoya disease; myotonic muscular dystrophy |
| MyD | myotonic dystrophy |
| MyMD | myotonic muscular dystrophy |
| ECCE | Extracapsular cataract extraction |
|---|---|
| PSC | Posterior subcapsular cataract |
| ICCE | intracapsular cataract extraction |
| CMD | Congenital myotonic dystrophy |
| MD | Myotonic Dystrophy |
| myotonic cataract | Cataract occurring in myotonic dystrophy. (05 Mar 2000) |
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| myotonic | Pertaining to or exhibiting myotonia. (05 Mar 2000) |
|---|---|
| myotonic dystrophy | <neurology> An inherited human neuromuscular disease classed as an autosomal dominant disease in which there is progressive muscle weakening and wasting. A triplet repeat syndromes (like fragile X syndrome), this most common adult form of muscular dystrophy is caused by expansion of the unstable trinucleotide repeat CTG in the 3' untranslated region on chromosome 19q13 (cAMP-dependent muscle protein kinase gene). Anticipation has been associated with further expansion of the repeat upon transmission to subsequent generations (the inheritance pattern is autosomal dominant), although contraction has been noted to occur as well. Especially severe neonatal cases have been born to affected mothers preferentially, suggesting a role for genomic imprinting as well. The classic physical signs include atrophy of facial muscles, cataracts, and delayed muscle relaxation. Detection of the expanded trinucleotide repeat is accomplished by PCR or Southern blot and expansion appears to correlate with decreased transcription of the protein kinase gene. Inheritance: autosomal dominant. (29 Dec 1997) |
| dystrophy, myotonic | Inherited disease with myotonia (irritability and prolonged contraction of muscles), mask-like face, premature balding, cataracts, and cardiac disease. Due to a trinucleotide repeat (a stuttering sequence of three bases) in the DNA. (12 Dec 1998) |
| annular cataract | Congenital cataract in which a central white membrane replaces the nucleus. Synonym: disk-shaped cataract, life-belt cataract, umbilicated cataract. (05 Mar 2000) |
| arborescent cataract | An obsolete term for dendritic cataract. (05 Mar 2000) |
| atopic cataract | A cataract associated with atopic dermatitis. (05 Mar 2000) |
| axial cataract | A lenticular opacity in the visual axis of the lens. (05 Mar 2000) |
| black cataract | A cataract in which the lens is hardened and of a dark brown colour. In the 19th century, German black cataract meant gutta severa (q.v.). Synonym: cataracta brunescens, cataracta nigra. (05 Mar 2000) |
| blue cataract | Coronary cataract of bluish colour. Synonym: cataracta cerulea. (05 Mar 2000) |
| capsular cataract | A cataract in which the opacity affects the capsule only. (05 Mar 2000) |
| capsulolenticular cataract | A cataract in which both the lens and its capsule are involved. See: membranous cataract. (05 Mar 2000) |
| galactose cataract | A neonatal cataract associated with intralenticular accumulation of galactose alcohol. See: galactosaemia. (05 Mar 2000) |
| radiation cataract | A cataract caused by excessive or prolonged exposure to ultraviolet rays, X-rays, radium, beta rays, gamma rays, heat, or radioactive isotopes. (05 Mar 2000) |
| vascular cataract | Congenital cataract in which the degenerated lens is replaced with mesodermal tissue. Synonym: cataracta adiposa, cataracta fibrosa. (05 Mar 2000) |
| reduplicated cataract | A type of congenital cataract with opacities situated at various levels in the lens. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|