| 영문 | hypersensitivity | 한글 | 과민, 예민 |
|---|---|---|---|
| 설명 | 1. 어떤 약물이나 자극에 대하여 과잉반응을 나타내는 방향으로 반응성이 변화한 상태. 과민성 반응은 면역반응에 의하여 생기는 병적 과정으로, 즉시형반응과 지연형반응으로 분류된다. 또한 다음의 4형으로 분류되기도 한다. I형은 즉시형 과민성 반응(예컨대 anaphylaxis). II형은 조직항원에 대한 항체에 의하여 생기는 손상(예컨대 콩팥독성 콩팥염). III형은 항원항체복합물, 특히 약간의 항원의 과잉에 의하여 형성되는 용해성 복합물에 의하여 생기는 것(예컨대 아르투스 반응이나 혈청병). IV형은 지연형 과미성 반응(예컨대 접촉성 피부병)이다. 2. 감각이나 감정이 지나치게 예민함. |
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| 영문 | immunological reaction | 한글 | 면역반응 |
|---|---|---|---|
| 설명 | 생체의 몸 안에서 생긴 물질이나 몸 밖에서 들어온 물질이 생체와 다를 때 자기 체내의 통일성과 개체의 생존 유지 및 종의 존속을 위하여 그 물질들을 제거하는 일련의 생체 반응. 다시 말해 B세포에 의한 항체생산, T세포를 중심으로 하는 세포성 면역, 면역관용, 면역기억 등의 생체 내 반응을 말한다. 큰포식세포는 항원을 처리해서 특이적인 항원결정기를 갖는 분자로 바꿔, 항원과 주요조직 적합유전자복합체를 세포표면에 표현하며, T세포로 전달한다. 한편 B세포는 큰포식세포 내에서 처리된 항원의 결정기를 인식하여 대응하는 특이적항체를 생산하여 항원을 처리한다. |
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| 영문 | reaction formation | 한글 | 반동형성, 반응형성 |
|---|---|---|---|
| 설명 | 억압보다 더 적극적인 방어메커니즘이며, 무의식적인 생각, 소원, 충동이 너무나도 받아들여질 수 없는 것일 경우에 이와는 정반대 방향의 것을 강조함으로써 그런 무의식적인 것들이 의식되지 않게 하는 과정. 예를 들면 가장 가학적인 성격의 사람이 생체해부 반대론자가 되는 경우를 들 수 있다. 이것은 또 가슴 깊이 잠겨있는 두려움이 의식되는 것을 피하기 위해서 두려움의 대상이 되는 행동에 골몰하는 경우도 포함이 된다. 예를 들면, 남자에게 상처받지 않을까 하는 두려움에 가득 찬 소녀가 이 같은 두려움을 부정하려는 수단으로 난잡한 성행위에 골몰하는 경우가 있다. 또 전처의 자녀를 미워하는 계모가 오히려 지나칠 정도로 그 아이를 귀여워하는 일 따위이다. |
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| 영문 | complement fixation reaction | 한글 | 보체결합 반응, 도움체결합반응 |
|---|---|---|---|
| 설명 | 항체와의 반응에 있어서 보체와 결합하는 항체를 검사하는 방법으로, 이 반응은 최초에 기지항원, 피검혈청 및 보체를 혼합한다. 제2단계에서는 적혈구와 이것에 대응하는 용혈소의 혼합액을 가한다. 본 반응후 용혈이 일어나지 않으면 본체는 항원항체결합물에 결합한 것이 되어 양성이 되지만, 용혈이 일어난 경우 보체는 결합하지 않아 소비되지 않기 때문에 음성이 된다. 본 반응은 기지혈청을 써서 항원검출에 응용할 수 있으며, 마이코플라스마, 리케챠, 클라미디아, 바이러스, 매독 등의 진단에 쓰인다. |
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| 영문 | transfusion reaction | 한글 | 수혈부작용, 수혈반응 |
|---|---|---|---|
| 설명 | 수혈하였을 때에 환자에게 일어나는 반응. 알레르기 반응과 용혈 반응이 있다. |
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| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
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| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| AT III | angiotensin III; antithrombin III |
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
| DTH | Delayed type hypersensitivity reaction |
|---|---|
| GSD III | Glycogen storage disease type III |
| HTLV III | Human T Cell Lymphotropic Virus Type III |
| HTLV-III | Human T-cell leukaemia virus type III |
| HTLV-III | Human T-lymphotropic virus type III |
| type III hypersensitivity reaction | An immunologic category of diseases evoked by the deposition of antigen-antibody or antigen-antibody-complement complexes on cell surfaces, with subsequent involvement of breakdown products of complement, platelets, and polymorphonuclear leukocytes, and development of vasculitis; nephritis is common. Arthus phenomenon and serum sickness are classic examples, but many other disorders, including most of the connective tissue disease's, may belong in this immunologic category; immune complex disease's can also occur during a variety of disease's of known aetiology, such as subacute bacterial endocarditis. See: autoimmune disease. Synonym: immune complex disorder, type III hypersensitivity reaction. (05 Mar 2000) |
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| delayed type hypersensitivity | <immunology> Hypersensitivity (increased reaction by the body to a foreign substance such as an antigen or allergen) that does not appear until 24 to 48 hours after the body is exposed to the foreign substance. (09 Oct 1997) |
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| tuberculin-type hypersensitivity | A local or generalised response that begins 24 to 48 hours after exposure to an antigen. See: cell-mediated reaction. Synonym: contact hypersensitivity, delayed hypersensitivity, late reaction, tuberculin-type hypersensitivity. (05 Mar 2000) |
| hypersensitivity reaction | <immunology> The bodys response to an allergic stimulus. This can be localised to one area or generalised and may include: rash, itching, hives, swelling, difficulty breathing, and/or low blood pressure. (27 Sep 1997) |
| immediate hypersensitivity reaction | An immune response mediated by antibody, usually IgE, which occurs within minutes after a second encounter with an antigen, resulting in the release of histamine and subsequent swelling and vasodilation. (05 Mar 2000) |
| glycogen storage disease type III | <disease> An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups type IIIa and type IIIb being the most prevalent. Inheritance: autosomal recessive (12 Dec 1998) |
| protoporphyrinogen type III | The immediate precursor of protoporphyrin III in haem biosynthesis; elevated in cases of variegate porphyria. (05 Mar 2000) |
| protoporphyrinogen type III oxidase | A mitochondrial enzyme that uses O2 to convert protoporphyrinogen type III to protoporphyrin type III in haem biosynthesis; a deficiency of this enzyme is associated with variegate porphyria. (05 Mar 2000) |
| protoporphyrin type III | 2,7,12,18-Tetramethyl-3,8-divinylporphin-13,17dipropionic acid;the principal protoporphyrin found in nature (one of 15 possible isomers), characterised by the presence of 4 methyl groups, 2 vinyl groups, and 2 propionic acid side chains; a porphyrin derivative that, with iron, forms the haem of haemoglobin and the prosthetic groups of myoglobin, catalase, cytochromes, etc. (05 Mar 2000) |
| hyperlipoproteinaemia type III | A rather uncommon form of familial hyperlipaemia characterised by the presence of lipoproteins of abnormal composition. The main abnormal lipoproteins are called beta-vldl and have a different apoprotein content and a higher proportion of cholesterol relative to triglyceride than normal vldl. (12 Dec 1998) |
| deoxyribonucleases, type III site-specific | <enzyme> Enzyme systems composed of two subunits and requiring ATP and magnesium for endonucleolytic activity; they do not function as atpases. They exist as complexes with modification methylases of similar specificity. The systems recognise specific short DNA sequences and cleave a short distance, about 24 to 27 bases, away from the recognition sequence to give specific double-stranded fragments with terminal 5'-phosphates. Enzymes from different microorganisms with the same specificity are called isoschizomers. Registry number: EC 3.1.21.5 (12 Dec 1998) |
| type III acrocephalosyndactyly | An autosomal dominant syndrome with variable expression of brachycephaly, maxillary hypoplasia, prominent ear crus, syndactyly, facial asymmetry, shallow orbits, telecanthus, and nasal septal deviation; may show mental retardation. Synonym: Saethre-Chotzen syndrome. (05 Mar 2000) |
| type III collagen | Collagen characteristic of reticular fibres. (05 Mar 2000) |
| type III familial hyperlipoproteinaemia | Hyperlipoproteinaemia characterised by increased plasma levels of LDL, beta-lipoproteins, pre-beta-lipoproteins, cholesterol, phospholipids, and triglycerides; hypertriglyceridemia induced by a high carbohydrate diet, and glucose tolerance is abnormal; frequent eruptive xanthomas and atheromatosis, particularly coronary artery disease; biochemical defect lies in apolipoproteins; there are many varieties. Synonym: carbohydrate-induced hyperlipaemia, dysbetalipoproteinaemia, familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia, familial hypercholesterolaemia with hyperlipaemia. (05 Mar 2000) |
| type III hyperlipoproteinaemia | <biochemistry> An inherited disorder (gene defect) where both cholesterol and triglycerides are elevated in the same patient. This condition accelerates the effects of atherosclerosis and thus increases the risk of cardiovascular disease. Conditions such as hypothyroidism, obesity and diabetes enhances this risk. Origin: Gr. Haima = blood (27 Sep 1997) |
| type III mucopolysaccharidosis | <syndrome> An error of the mucopolysaccharide metabolism, with excretion of large amounts of heparan sulfate in the urine and severe mental retardation with hepatomegaly; skeleton may be normal or may present mild changes similar to those in Hurler's syndrome; several different types (A, B, C, and D) have been identified according to the enzyme deficiency; autosomal recessive inheritance. Synonym: type III mucopolysaccharidosis. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|