| 영문 | motor unit | 한글 | 운동단위 |
|---|---|---|---|
| 설명 | 운동을 이루는 단위를 묶어 말한다. 즉, 운동을 유발시키는 척수의 앞뿔세포(운동신경이 주로 모여 있는 곳으로 뇌에서 전달된 운동이 수행되도록 근육에 전달시키는 역할을 한다), 전달신경축삭, 말단 신경-근육 접합부, 그리고 운동을 실제 이루는 근육 등을 모두 묶어 이르는 말이다. |
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| 영문 | intensive care unit | 한글 | 중환자실 |
|---|---|---|---|
| 설명 | 병세나 상처 따위의 정도가 매우 심한 사람을 치료하고 돌볼 수 있도록 마련한 방. 호흡-순환-대사 등 정신적 급성기능상실의 환자를 취급하며 강력하고도 집중적인 진료를 하는 부분이다. 위독한 환자에 대하여는 24시간 체제로 대응한다. 충분히 훈련을 받은 의료진이 배치되며 기능적으로 설비가 갖추어져 있다. 심근경색증-호흡기능상실-콩팥기능상실-소아-신경외과계 등 특정환자를 대상으로 한다. |
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| EU | Ehrlich unit; elementary unit; emergency unit; endotoxin unit; entropy unit; enzyme unit; esterase u... |
|---|---|
| CU | cardiac unit; casein unit; cause unknown or undetermined; chymotrypsin unit; clinical unit; color un... |
| HU | heat unit; hemagglutinating unit; hemolytic unit; Hounsfield unit; human urine, human urinary; hydro... |
| TU | thiouracil; thyroid uptake; Todd unit; toxin unit; transmission unit; transurethral; tuberculin unit... |
| AU | according to custom [Lat. ad usum]; allergenic unit; ngstrom unit; antitoxin unit; arbitrary unit; A... |
| AIHA | Auto-immune haemolytic anaemia |
|---|---|
| AHA | autoimmune haemolytic anaemia |
| GABHS | Group A beta haemolytic streptococcus |
| GABHS | Group A beta-haemolytic streptococci |
| GAS | Group A beta-haemolytic streptococci |
| haemolytic unit | The smallest quantity (highest dilution) of inactivated immune serum (haemolysin) that will sensitise the standard suspension of erythrocytes so that the standard complement will cause complete haemolysis. Synonym: amboceptor unit. (05 Mar 2000) |
|---|
| ABO haemolytic disease of the newborn | Erythroblastosis foetalis due to maternal-foetal incompatibility with respect to an antigen of the ABO blood group; the foetus possesses A or B antigen which is lacking in the mother, and the mother produces immune antibody which causes haemolysis of foetal erythrocytes. (05 Mar 2000) |
|---|---|
| acquired haemolytic anaemia | Nonhereditary acute or chronic anaemia associated with or caused by extracorpuscular factors, e.g., certain infectious agents, chemicals (including autoantibodies or therapeutic agents), burns, toxic materials from higher plant and animal forms (including snake venoms). (05 Mar 2000) |
| acquired haemolytic icterus | Icterus and anaemia occuring in association with a moderate degree of splenomegaly, increased fragility of red blood cells, and increased amounts of urobilin in the urine. Synonym: icteroanaemia. Origin: G. Ikteros (05 Mar 2000) |
| anaemia, haemolytic | Anaemia due to decreased life span of erythrocytes. (12 Dec 1998) |
| anaemia, haemolytic, autoimmune | Acquired haemolytic anaemia due to the presence of autoantibodies which agglutinate or lyse the patient's own red cells. (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) |
| angiopathic haemolytic anaemia | A rare postpartum anaemia of unknown aetiology with uraemia and nephrosclerosis; may be a rare complication following use of contraceptive steroids. (05 Mar 2000) |
| autoimmune haemolytic anaemia | <haematology> A condition that results from the cellular destruction (haemolysis) of red blood cells due to antibodies formed to components on the surface of the red blood cells. Origin: Gr. Haima = blood (02 Jan 1998) |
| beta-haemolytic streptococci | Those that produce active haemolysins (O and S) which cause a zone of clear haemolysis on the blood agar medium in the area of the colony; beta-haemolytic streptococci are divided into groups (A to O) on the basis of cell wall C carbohydrate (see Lancefield classification); Group A (in the strains pathogenic for man) comprises more than 50 types (designated by Arabic numerals) determined by cell wall M protein, which seems to be associated closely with virulence and is produced chiefly by strains with matt or mucoid colonies, in contrast to nonvirulent, glossy colony-producing strains; other surface protein antigens such as R and T (T substance), and the nucleoprotein fraction (P substance) seem to be of less importance. The more than 20 extracellular substances elaborated by strains of beta-haemolytic streptococci include erythrogenic toxin (elaborated only by lysogenic strains), deoxyribonuclease (streptodornase), haemolysins (streptolysins O and S), hyaluronidase, and streptokinase. Synonym: haemolytic streptococci. (05 Mar 2000) |
| microangiopathic haemolytic anaemia | <haematology> Consequence of disseminated intravascular coagulation (DIC): fragments of red blood cells, damaged by being forced through a fibrin meshwork, are found in the circulation. Origin: Gr. Haima = blood (18 Nov 1997) |
| complement haemolytic activity assay | Usual screening assay for complement. Dilutions of the serum to be tested are added to antibody-coated erythrocytes and the percentage of lysis is measured. The values are expressed by ch50, haemolytic complement units per milliliter, which is the dilution of serum required to lyse 50 percent of the erythrocytes in the assay. (12 Dec 1998) |
| congenital haemolytic anaemia | Accelerated destruction of red blood cells due to an inherited defect, such as in the membrane in hereditary spherocytosis. (05 Mar 2000) |
| congenital haemolytic icterus | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
| congenital haemolytic jaundice | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|