| 영문 | retinal detachment | 한글 | 망막 박리 |
|---|---|---|---|
| 설명 | 카메라에 있어서 필름에 해당하는 눈의 망막은 크게 두 개의 층으로 나눌 수가 있다. 안쪽에 있는 실제의 빛을 감지하는 감각층과 바깥쪽의 외부의 빛을 차단하는 색소상피층이 그것인데 그 사이에는 잠재적인 공간이 있어서 떨어지기가 쉽다. 이 사이가 떨어지면 망막의 감각층이 망막의 색소상피층과 분리되는데 이것을 망막박리라고 한다. 이 망막의 박리에는 여러 가지 원인이 있지만 감각층의 망막에 작은 구멍인 열공(break)에 의해서 그곳으로 눈속을 채우고 있는 액체가 흘러 들어가서 생기는 망막의 박리를 열공성 망막박리(rhegmatogenous retinal detachment)라 하고, 안구의 병터에 의해서 안구내에 섬유조직이 생기고 그것이 망막의 감각층을 잡아 끌어서 망막이 박리되는 견인성 망막박리(traction retinal detachment) 및 망막의 2개의 층에 삼출액이 괴어서 생기는 삼출성 망막박리(exudative retinal detachment) 등 열공에 의해서 생기는 망막박리가 아닌 것을 비열공성 망막박리(nonrhegmatogenous retinal detachment)라고 말한다. |
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| MURCS Associations | MUllerian duct aplasia, Renal aplasia, Cervico-thoracic vertebral(Somite) dysplasia Associations |
|---|---|
| RD | radial deviation; radiology department; rate difference; Raynaud disease; reaction of degeneration; ... |
| PRCA | Pure Red Cell Aplasia |
| ACC | accommodation; acetyl coenzyme A carboxylase; acinic cell carcinoma; acute care center; adenoid cyst... |
| ARCA | acquired red cell aplasia |
| ACC | Aplasia cutis congenita |
|---|---|
| PRCA | Pure Red Cell Aplasia |
| ARN | Acute retinal necrosis |
| ARN | Acute retinal necrosis syndrome |
| ARC | Anomalous retinal correspondence |
| aplasia | <embryology> A lack of development of an organ or tissue or of the cellular products from an organ or tissue. Compare: hypoplasia. Origin: Gr. Plassein = to form (18 Nov 1997) |
|---|---|
| aplasia cutis congenita | Congenital absence or deficiency of a localised area of skin, with the base of the defect covered by a thin translucent membrane; most often a single area near the vertex of the scalp, but may occur in other areas; underlying structures may also be affected; autosomal inheritance, either dominant or recessive. (05 Mar 2000) |
| radial aplasia-thrombocytopenia syndrome | <syndrome> Aplasia (absence) of the radius (the long bone on the thumb-side of the forearm) and thrombocytopenia (low blood platelets) are key features characterizing this syndrome. There is phocomelia (flipper-limb) with the thumbs always present. The fibula (the smaller bone in the lower leg) is often absent. The risk of bleeding from too few platelets is high in early infancy but lessens with age. The condition is inherited in an autosomal recessive trait with one gene (on a non-sex chromosome) coming from each parent to the child affected with the disease. Alternative names include thrombocytopenia-absent radius syndrome, tar syndrome, and tetraphocomelia-thrombocytopenia syndrome. (12 Dec 1998) |
| germinal aplasia | A disorder in which the seminiferous tubules exhibit an abnormal cytoarchitecture and extensive hyalinization; the testes are small, and few spermatozoa are formed; the body habitus may be eunuchoid, and gynaecomastia may be present; urinary gonadotropin output is usually high, and the incidence of mental deficiency and illness increased; sex chromatin may be male or female, and androgen secretion ranges from subnormal to normal. It is a constant feature of (and is often used synonymously with) Klinefelter's syndrome. Synonym: germinal aplasia. (05 Mar 2000) |
| red-cell aplasia, pure | Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. (12 Dec 1998) |
| gonadal aplasia | Congenital absence of essentially all gonadal tissue; the external genitalia and genital ducts are female, but if interstitial cells of Leydig are present, the external genitalia are commonly ambiguous and the genital ducts are female. See: gonadal dysgenesis. Compare: Klinefelter's syndrome, Turner's syndrome. Synonym: gonadal agenesis. (05 Mar 2000) |
| congenital aplasia of thymus | diGeorge syndrome |
| pure red cell aplasia | A transitory arrest of red blood cell production which may occur in the course of a haemolytic anaemia, often preceded by infection, or as a complication of certain drugs; if the arrest persists anaemia may result. See: congenital hypoplastic anaemia. (05 Mar 2000) |
| syndrome, radial aplasia-thrombocytopenia | See syndrome, tar. (12 Dec 1998) |
| thymic aplasia | <disease, immunology> A lack of T lymphocytes, due to failure of the thymus to develop, resulting in very reduced cell-mediated immunity though serum immunoglobulin levels may be normal. See: DiGeorge syndrome. Origin: Gr. Plassein = to form (18 Nov 1997) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|