| 영문 | Rorschach Test | 한글 | 로르샤하 검사 |
|---|---|---|---|
| 설명 | 사고장애와 정서장애에 민감한 투사검사(projective test). 검은색과 몇가지 색으로 이루어진 잉크얼룩같은 도형이 그려진 10개의 카드를 이용한다. 피검자에게 카드를 보이고 본 것에 대해 말하도록 한다. 다음에는 얼룩의 어느 위치가 피검자가 말한 지각대상을 암시하는지 찾도록 한다. 피검자의 답변을 분석하면 그의 사고와 정서상태에 대한 정보를 얻을 수 있다. |
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| 영문 | Mantoux test | 한글 | 망토우검사 |
|---|---|---|---|
| 설명 | 소아에 주로 실시하는 검사 방법으로, BCG접종후에나 혹은 결핵균에 한번이라도 노출된 경우에 양성반응으로 나온다. 우리나라에서는 생후 1개월에 BCG예방접종을 시행하므로 대부분 양성으로 나오게 되나, 이 예방접종을 받지 않은 상태에서 양성으로 나오면, 결핵균의 침투를 의심할 수 있다. |
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| 영문 | stress test | 한글 | 스트레스 검사 |
|---|---|---|---|
| 설명 | 협심증이 일어나기 쉬운 환자에게서 그 정도를 판단하기위해 시행한다. 방법은 같은 곳에서 환자를 달리도록 한 다음, 얼마의 속도에서 혈압이 떨어지고 협심증 증상이 나타나는가를 검사한다. 대개 심할수록 낮은 속도에서도 증상이 빨리 나타난다. |
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| 영문 | visual field test | 한글 | 시야검사 |
|---|---|---|---|
| 설명 | 눈을 한곳에 고정시킨 채, 관찰할 수 있는 주변공간을 시야라 한다. 시야를 검사하는 가장 간단한 방법은 대면검사(confronting test)이다. 이것은 피검사자의 눈을 검사자의 눈에 맞추어 보도록 하여 눈을 고정시킨채, 검사자가 손가락끝을 위쪽, 아래쪽, 왼쪽, 오른쪽, 그리고 비스듬히 경사진 곳 등으로 옮겨보아 피검사자가 관찰할 수 있는지 여부를 정하는 검사법이다. 이보다 정확한 검사법은 자동식 컴퓨터시야검사법이 있다. 대개, 눈자체의 이상이 있어도 시야검사에서 이상이 나오지만, 이외 뇌의 이상으로 시각의 형성경로에 이상이 있어도 역시 이상소견을 보인다. |
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| 영문 | Draw a person test | 한글 | 인물화 성격검사 |
|---|---|---|---|
| 설명 | 인물화 성격검사는 처음에는 지능검사로 개발되었고, 그 후에는 사람의 무의식의 요소를 검사하는 방법으로 발전하였다. 검사재료는 지우개가 있는 연필과 백지를 피검자에게 주고, 사람을 그려보라는 지시를 하며, 검사자는 그리는 순서와 평가를 기록하고, 다 그린 후에는 먼저와 다른 이성을 그리도록 한다. 이 검사에서의 신체의 모양은 곧 자아상을 반영한다는 입장, 그림에서 강조된 기관은 의사소통수단, 관념화, 욕구체계, 성적 능력, 갈등, 좌절경험, 성장력 등을 반영한다고 한다. 이것은 아동과 성인에게 개별적 또는 집단적으로 실시할 수 있고, 간편하면서도 유익한 것이다. 임상적으로는 뇌의 기질적 변화를 알아내기 위한 목적으로도 많이 이용된다. |
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| DAT | delayed-action tablet; dementia Alzheimer's type; dental aptitude test; diacetylthiamine; diet as to... |
|---|---|
| IT | immunological test; immunotherapy; implantation test; individual therapy; information technology; in... |
| LFT | latex fixation test; latex flocculation test; left fronto-transverse [fetal position]; liver functio... |
| LTT | lactose tolerance test; leucine tolerance test; limited treadmill test; lymphocyte transformation te... |
| SAT | saliva alcohol test; satellite; serum antitrypsin; single-agent chemotherapy; slide agglutination te... |
| glucose-1-phosphatase | <enzyme> Catalyses the conversion of d-glucose 1-phosphate and water to d-glucose and orthophosphate Registry number: EC 3.1.3.10 Synonym: agp gene product (26 Jun 1999) |
|---|---|
| glucose 1-phosphate | <biochemistry> Product of glycogen breakdown by phosphorylase. Converted to glucose 6 phosphate by phosphoglucomutase. (18 Nov 1997) |
| glucose-1-phosphate adenylyltransferase | <enzyme> Shrunken-2 (sh2) protein is a subunit of this enzyme Registry number: EC 2.7.7.27 Synonym: adpg synthetase, adpglucose pyrophosphorylase, ADP-glucose synthetase, shrunken-2 protein, shrunken gene product, ADP-glucose pyrophosphorylase, glgc gene product, bt2 gene product, brittle-2 gene product (26 Jun 1999) |
| glucose-1-phosphate kinase | <enzyme> An enzyme that, in the presence of ATP, catalyses the phosphorylation of d-glucose 1-phosphate to form d-glucose 1,6-bisphosphate and ADP; found in yeast and muscle; d-glucose 1,6-bisphosphate is a required cofactor of one of the enzymes in glycogenolysis. Synonym: glucose-1-phosphate kinase. (05 Mar 2000) |
| glucose-1-phosphate phosphodismutase | A phosphotransferase catalyzing the reversible transfer of a phosphate residue from one d-glucose 1-phosphate to another, yielding d-glucose 1,6-bisphosphate and d-glucose. This enzyme provides a crucial intermediate needed for glucose-phosphate isomerase. (05 Mar 2000) |
| glucose-1-phosphate uridylyltransferase | <enzyme> An enzyme that activates d-glucose by reacting d-glucose 1-phosphate with UTP, producing pyrophosphate and UDP glucose; a crucial step in glycogen biosynthesis. (05 Mar 2000) |
| glucose-1-phospho-D-mannosylglycoprotein phosphodiesterase | <enzyme> Removes the glucose-1-phosphate from glc-alpha-1-p-6-mannose residues in glycoproteins as a unit; pH optimum 7.5 Registry number: EC 3.1.4.51 Synonym: ag1p phosphodiesterase, alpha-glucose-1-phosphate phosphodiesterase (26 Jun 1999) |
| glucose-3-phosphatase | <enzyme> From rat liver; has glucose-3-phosphate hydrolytic activity Registry number: EC 3.1.3.- (26 Jun 1999) |
| glucose-6-dehydrogenase deficiency | <biochemistry> An inherited condition that results in a deficiency in glucose-6-phosphate dehydrogenase. Particular drugs (sulphonamides) can exacerbate this problem. The result is haemolytic anaemia. (27 Sep 1997) |
| glucose-6-phosphatase | <enzyme> An enzyme that catalyses the conversion of d-glucose-6-phosphate and water to d-glucose and orthophosphate. This enzyme is deficient in glycogen storage disease Ia. Chemical name: D-Glucose-6-phosphate phosphohydrolase Registry number: EC 3.1.3.9 (12 Dec 1998) |
| glucose-6-phosphatase hepatorenal glycogenosis | Glycogenosis due to glucose-6-phosphatase deficiency, resulting in accumulation of excessive amounts of glycogen of normal chemical structure, particularly in liver and kidney. Synonym: Gierke's disease, glucose-6-phosphatase hepatorenal glycogenosis, von Gierke's disease. (05 Mar 2000) |
| glucose-6-phosphate | <biochemistry> Glucose 6-phosphate is a phosphomonoester of glucose that is formed by transfer of phosphate from ATP, catalysed by the enzyme hexokinase. It is an intermediate both of the glycolytic pathway (next converted to fructose 6 phosphate) and of the NADPH generating pentose phosphate pathway, formed from glucose via hexokinase. However it is not strictly a glycolytic intermediate and it is readily converted to glycogen or oxidized to NADPH. (10 Oct 1997) |
| glucose-6-phosphate dehydrogenase | <enzyme> An NADP+ enzyme that catalyses the dehydrogenation (oxidation) of d-glucose-6-phosphate to 6-phospho-d-glucono-d-lactone, this reaction initiating the Dickens shunt. Deficiency of this enzyme is the commonest disease-causing enzyme defect in humans affecting an estimated 400 million people. The gene for this enzyme is on the X chromosome. Males with the enzyme deficiency develop haemolytic anaemia when red blood cells are exposed to oxidant drugs such as the antimalarial primaquine, the sulfonamide antibiotics or sulfones, naphthalene moth balls, or fava beans. Synonym: Robison ester dehydrogenase, Zwischenferment. Acronym: G6PD (12 Sep 2002) |
| glucose-6-phosphate dehydrogenase deficiency | A deficiency of glucose-6-phosphate dehydrogenase, an enzyme important for maintaining cellular concentrations of reduced nucleotides. Deficiency of this enzyme is the commonest disease-causing enzyme defect in humans affecting an estimated 400 million people. The gene for this enzyme is on the X chromosome and there are various polymorphic forms. Males with the enzyme deficiency develop haemolytic anaemia when red blood cells are exposed to oxidant drugs such as the antimalarial primaquine, the sulfonamide antibiotics or sulfones, naphthalene moth balls, or fava beans. It can also cause anaemia of the newborn, and chronic nonspherocytic haemolytic anaemia. Inheritance: X-linked. (12 Sep 2002) |
| glucose-6-phosphate isomerase | <enzyme> An enzyme that catalyses the reversible interconversion of glucose-6-phosphate and fructose-6-phosphate, and is a part of the glycolytic and gluconeogenic pathways. Deficiency of the enzyme, an autosomal recessive trait, results in liver glycogenesis and haemolytic anaemia. Chemical name: D-Glucose-6-phosphate ketol-isomerase Registry number: EC 5.3.1.9 (12 Dec 1998) |