| 영문 | ultraviolet | 한글 | 자외선 |
|---|---|---|---|
| 설명 | 보라색보다 더욱 파장이 짧은 400nm 이하의 볼 수 없는 광선이며 다음의 3종으로 나눈다. ① 200~290nm(UVC): 저압램프에서 조사되는 것으로 DNA를 저해하며 피부에 조사되면 홍반이 생긴다. 대기중의 O3나 H2O에서 흡수된다. ② 290~320nm(UVB): 피부가 햇볕에 타서 검게 되며 지나치면 수포나 피부암을 일으킬 위험이 있다. ③ 320~400nm(UVA): 지표면에 많으며 무해하다. 다량이 폭로되면 피부에 색소침착을 일으킨다. |
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| 영문 | ultraviolet B | 한글 | 중간파장자외선 |
|---|---|---|---|
| 설명 | 290~320nm의 자외선. 일광화상과 그을림을 가장 효과적으로 유발한다. 백인에서 자외선 과다는 피부암을 유발할 수 있다. |
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| 영문 | ultraviolet C | 한글 | 짧은파장자외선 |
|---|---|---|---|
| 설명 | 200~290nm의 자외선 방사. UVC라고도 한다. 일광의 UVC는 지구 표면에 도달하지 않는다. 멸균/수은아크등은 일광화상과 각막염을 유발할 수 있다. |
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| 영문 | basal layer of skin | 한글 | 기저층 |
|---|---|---|---|
| 설명 | 표피의 가장 아래 부분이며 세포의 모양이 비교적 직사각형에 가깝고 일정한 배열을 한다. |
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| 영문 | radiation | 한글 | 방사선 |
|---|---|---|---|
| 설명 | 빛의 전자자기파나 혹은 입자파(α, β, γ선)를 말하는데, 어떤 근원물질에서 생겨 방출된다. 이온쌍을 생성하는 고에너지 방사선(X-선과 감마선)을 말한다. 방사선하면, 주로 전리방사선을 의미한다. 이런 방사선을 이용하여, 가장 기본적인 방사선학적 검사를 할 수 있으며, 이외 치료에도 이용하고 있다. 각 방사선의 종류에 따라 조금씩 인체에 미치는 영향이 다르며, 이를 이용하여 각기 다르게 진단 및 치료에 이용한다. |
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| AML | Acute Myelogenous Leukemia Morphologic Classification(FAB분류) &n... |
|---|---|
| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
| AML | acute monocytic leukemia; acute mucosal lesion; acute myeloblastic leukemia; acute myelocytic leukem... |
| AP | accessory pathway; accounts payable; acid phosphatase; acinar parenchyma; action potential; active p... |
| KW change | Keith Wagener change |
| UVB | Ultraviolet B radiation |
|---|---|
| UVR | Ultraviolet B radiation |
| UV | Ultraviolet radiation |
| UVA | Ultraviolet-A radiation |
| DUE | DNA unwinding element |
acute angle
acute arthritis
acute monocytic leukemia
| ultraviolet radiation | <physics> Invisible light, next to visible light in the electromagnetic spectrum. The most common source of ultraviolet radiation is the sun. Acronym: UV (16 Dec 1997) |
|---|---|
| due date | The estimated calendar date when a baby will be born, the date the baby is due to be born. It is also called the estimated date of confinement (EDC). (12 Dec 1998) |
| dystonia, focal, due to blepharospasm | The second most common focal dystonia, the involuntary, forcible closure of the eyelids. The first symptoms may be uncontrollable blinking. Only one eye may be affected initially, but eventually both eyes are usually involved. The spasms may leave the eyelids completely closed causing functional blindness even though the eyes and vision are normal. (12 Dec 1998) |
| dystonia, focal, due to torticollis | Spasmodic torticollis, or torticollis, is the most common of the focal dystonias. In torticollis, the muscles in the neck that control the position of the head are affected, causing the head to twist and turn to one side. In addition, the head may be pulled forward or backward. (12 Dec 1998) |
| thrombotic disease due to protein c deficiency | Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein c results in thrombotic (clotting) disease and excess platelets with recurrent thrombophlebitis (inflammation of the vein that occurs when a clot forms). The clot can break loose and travel through the blood stream (thromboembolism) to the lungs causing a pulmonary embolism, brain causing a stroke (cerebrovascular accident), heart causing an early heart attack, skin causing what in the newborn is called neonatal purpura fulminans, the adrenal gland causing haemorrhage with abdominal pain, abnormally low blood pressure (hypotension), and salt loss. Protein c deficiency is due to possession of one gene (heterozygosity) in chromosome band 2q13-14. The possession of two such genes (homozygosity) is usually lethal. (12 Dec 1998) |
| acute radiation syndrome | <syndrome> A syndrome caused by exposure of the body to large amounts of radiation, (e.g., from certain forms of therapy, accidents, and nuclear explosions; it is divided into three major forms which are, in ascending order of severity, the haematogic, gastrointestinal, and central nervous system-cardiovascular forms; its clinical manifestations are divided into prodromal, latent, overt, and recovery stages. (05 Mar 2000) |
| infantile acute haemorrhagic oedema of the skin | A generally benign form of cutaneous vasculitis, characterised by ecchymotic purpura, often in a cockade pattern, and inflammatory oedema in infants. (05 Mar 2000) |
| Armanni-Ebstein change | Glycogen vacuolization of the loops of Henle, seen in diabetics before the introduction of insulin. Synonym: Armanni-Ebstein change. (05 Mar 2000) |
| Baggenstoss change | Distention of pancreatic acini by proteinaceous secretion, seen in dehydration. (05 Mar 2000) |
| change | An alteration; in pathology, structural alteration of which the cause and significance is uncertain. Synonym: shift. (05 Mar 2000) |
| change of life | Colloquialism for menopause, climacteric. (05 Mar 2000) |
| chemical change | A process in which one or more substances are changed into one or more different substances. (09 Oct 1997) |
| minimal-change disease | <nephrology> A disorder of the kidneys which largely affects the glomerulus, the blood filtering structure. This disorder is one common cause of nephrotic syndrome, minimal glomerular changes, in children affecting 2 to 3 children per 100,000 population under age 16 in the USA. Minimal change disease is also seen rarely in adults. The cause is unknown but may be related to an autoimmune illness. It is marked by oedema, albuminuria, and an increase in cholesterol in the blood, but otherwise with fairly good renal function. Tubular epithelium is vacuolated by cholesterol droplets, but the glomeruli show only that the foot processes of the glomerular epithelial cells are fused, probably secondary to the proteinuria; the cause of the increased glomerular permeability to plasma protein is unknown. Risk factors include a history for a immune disorder, recent immunisation or a bee sting. Diagnosis is made by renal biopsy. Treatment include systemic corticosteroids which are usually quite effective in curing this disease. Other medications include chlorambucil and cyclophosphamide. In most cases, a moderate protein diet (1 gram protein per Kg body weight per day) will be recommended. Salt (sodium) restriction can be helpful to reduce swelling and vitamin D is usually supplemented. Synonym: lipoid nephrosis (27 Sep 1997) |
| minimal-change nephrotic syndrome | <nephrology> A disorder of the kidneys which largely affects the glomerulus, the blood filtering structure. This disorder is one common cause of nephrotic syndrome, minimal glomerular changes, in children affecting 2 to 3 children per 100,000 population under age 16 in the USA. Minimal change disease is also seen rarely in adults. The cause is unknown but may be related to an autoimmune illness. It is marked by oedema, albuminuria, and an increase in cholesterol in the blood, but otherwise with fairly good renal function. Tubular epithelium is vacuolated by cholesterol droplets, but the glomeruli show only that the foot processes of the glomerular epithelial cells are fused, probably secondary to the proteinuria; the cause of the increased glomerular permeability to plasma protein is unknown. Risk factors include a history for a immune disorder, recent immunisation or a bee sting. Diagnosis is made by renal biopsy. Treatment include systemic corticosteroids which are usually quite effective in curing this disease. Other medications include chlorambucil and cyclophosphamide. In most cases, a moderate protein diet (1 gram protein per Kg body weight per day) will be recommended. Salt (sodium) restriction can be helpful to reduce swelling and vitamin D is usually supplemented. Synonym: lipoid nephrosis (27 Sep 1997) |
| conformational change | <cell biology> Alteration in the shape usually the tertiary structure of a protein as a result of alteration in the environment pH, temperature, ionic strength) or the binding of a ligand (to a receptor) or binding of substrate (to an enzyme). (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|