| 영문 | amino acids | 한글 | 아미노산 |
|---|---|---|---|
| 설명 | 아미노기(－NH3)와 카르복실기(－COOH)를 가지고 있는 모든 유기물질. 단백질을 이루는 기본단위가 된다. 즉 단백질은 아미노산이 연결되어서 이루는 것이다. 인체에서는 아미노산이 단백질의 기본단위가 되는 것외에 신경세포와 신경세포가 서로 연락을 주고 받는데 쓰이는 신경전달물질로서의 역할도 한다. 사람의 단백질은 20가지의 아미노산으로 구성된다. 즉 사람에 있어서 단백질을 합성하는 데는 20가지의 아미노산이 필요하다. 여기에서 11가지는 인체내에서 직접 합성할 수 있지만 나머지 9가지는 합성할 수 없고 반드시 음식물에서 섭취해야 한다. 이것을 필수아미노산이라고 한다. |
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| 영문 | renal biopsy | 한글 | 콩팥생검 |
|---|---|---|---|
| 설명 | 콩팥의 병변이 의심될 때 확진을 위해 주사바늘 등을 이용하여 콩팥조직을 일부 떼어내서 현미경으로 검경하는 것. |
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| 영문 | renal hypertension | 한글 | 콩팥성고혈압 |
|---|---|---|---|
| 설명 | 콩팥실질의 병변으로 인해 야기된 고혈압. 콩팥의 대표적 기능은 노폐물 및 수분의 배설이다. 그런데 이러한 콩팥기능에 이상이 생겼을 경우 체내에 과잉수분의 축적이 발생하게 된다. 이와같은 과잉수분의 축적은 혈관내 정수압을 상승시켜 고혈압을 유발하게 된다. 치료는 원인 콩팥병의 교정이며 이유를 모르는 원발고혈압과 달리 콩팥성고혈압의 경우에는 원인 콩팥병이 교정되면 고혈압도 사라지게 된다. |
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| 영문 | renal cell carcinoma | 한글 | 콩팥세포암종 |
|---|---|---|---|
| 설명 | 콩팥에 생긴 원시콩팥조직에서 발생한 암. 주로 원시세뇨관조직에서 발생한다. 대표적인 세포조직형은 염색시 세포질이 맑게 비어보이는 맑은세포암종이다. 치료는 수술과 항암화학요법이며 아주 드물지만 저절로 낫는 경우도 있는 것으로 보고되어 있다. |
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| 영문 | renal transplantation | 한글 | 콩팥이식 |
|---|---|---|---|
| 설명 | 콩팥병을 가지고 있으나 치료가 불가능한 만성콩팥기능상실 등의 질병을 가진 환자의 신장을 떼어내고 환자와 항원성이 유사한 사람의 콩팥을 이식해주는 것. 이 때 서로간의 항원성의 유사점이 많아야 거부반응이 일어나지 않는다. 그리고 일단 콩팥이식을 받은 사람은 오랜기간 동안 면역억제제를 투여하여 거부반응을 줄여야 한다. 대개 이식된 콩팥은 엉덩뼈오목에 위치하게 된다. |
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| AAN | AIDS-associated nephropathy; alpha-amino nitrogen; American Academy of Neurology; American Academy o... |
|---|---|
| EAA | electroacupuncture analgesia; Epilepsy Association of America; essential amino acid; excitatory amin... |
| CRD | carbohydrate-recognition domain; chronic renal disease; chronic respiratory disease; child restraint... |
| CRT | cadaveric renal transplant; cardiac resuscitation team; cathode-ray tube; certified; Certified Recor... |
| RVRA | renal vein rein activity; renal venous renin assay |
| GA I | Glutaric aciduria type I |
|---|---|
| MMA | Methylmalonic aciduria |
| ARI | 5--acute renal insufficiency |
| ARCD | Acquired renal cystic disease |
| ARF | Acute Renal Failure |
beta-arrestin
para-amino salicylic acid
| aciduria | 1. Excretion of an acid urine. 2. Excretion of an abnormal amount of any specified acid. Individual types of aciduria are prefixed by the specific acid; e.g., aminoaciduria, ketoaciduria. Origin: acid + G. Ouron, urine (05 Mar 2000) |
|---|---|
| argininosuccinic aciduria | <biochemistry> Argininosuccinic aciduria, an autosomal recessive defect of the urea cycle, is due to deficiency of argininosuccinate lyase (argininosuccinase), which catalyses the hydrolysis of argininosuccinic acid to arginine and fumaric acid. It is characterised by excessive urinary excretion of argininosuccinic acid, epilepsy, ataxia, mental retardation, liver disease, and friable, tufted hair; presumed to be the consequence of a deficiency of an enzyme responsible for splitting argininosuccinic acid to arginine and fumaric acid. Argininosuccinase is a cytosolic enzyme found in highest amounts in the liver. Like the other urea cycle defects except for arginase deficiency, argininosuccinic aciduria typically presents early in the neonatal period with serious, often fatal, hyperammonaemia and residual neurologic damage. Argininosuccinic acid is found in high concentrations in plasma and urine by amino acid chromatography. It can also be detected in amniotic fluid for purposes of prenatal diagnosis. Diagnosis is confirmed by specific enzyme assay. The argininosuccinase gene has been cloned and is found on chromosome 7. Inheritance: autosomal recessive. Acronym: ASA (05 Mar 2000) |
| beta-hydroxypropionic aciduria | Elevated levels of beta-hydroxypropionic acid in the urine; seen in defects in methylmalonic acid and propionate metabolism, as well as in ketotic hyperglycinaemia syndrome. (05 Mar 2000) |
| glycolic aciduria | Excessive excretion of glycolic acid in the urine; a primary metabolic defect due to deficiency of 2-hydroxy-3-oxoadipate carboxylase, resulting in excretion of glycolic and oxalic acids, leading to the clinical syndrome of oxalosis. (05 Mar 2000) |
| methylmalonic aciduria | Excretion of excessive amounts of methylmalonic acid in urine owing to deficient activity of methylmalonyl-CoA mutase or deficient cobalamin reductase. Two types occur: 1) an inborn error of metabolism resulting in severe ketoacidosis shortly after birth, with long-chain urinary ketones; autosomal recessive inheritance; 2) acquired, a type due to vitamin B12 deficiency due to defective synthesis of adenosylcobalamin. (05 Mar 2000) |
| mevalonic aciduria | Elevated levels of mevalonic acid in the urine; associated with a deficiency of mevalonate kinase. (05 Mar 2000) |
| hyper-beta-aminoisobutyric aciduria | Elevated levels of beta-aminoisobutyric acid in the urine; believed to be due to a deficiency of liver R-beta-aminoisobutyrate:pyruvate aminotransferase. (05 Mar 2000) |
| d-glyceric aciduria | 1. Elevated levels of d-glyceric acid in the urine. 2. An inborn error in metabolism resulting in d-glyceric aciduria. (05 Mar 2000) |
| orotic aciduria | A rare disorder of pyrimidine metabolism characterised by hypochromic anaemia with megaloblastic changes in bone marrow, leukopenia, retarded growth, and urinary excretion of orotic acid; autosomal recessive inheritance. Origin: orotic acid + G. Ouron, urine (05 Mar 2000) |
| urocanic aciduria | Elevated levels of urocanic acid in the urine. (05 Mar 2000) |
| 3-methylglutaconic aciduria | Elevated levels of 3-methylglutaconic acid in the urine. An inherited disorder whose mild form is a result of a deficiency of 3-methylglutaconyl-CoA hydratase, leading to delayed speech development. (05 Mar 2000) |
| 4-hydroxybutyric aciduria | Elevated levels of 4-hydroxybutyrate in the urine. An inherited disorder that can lead to hypotonia and mental retardation. (05 Mar 2000) |
| l-glyceric aciduria | Excretion of l-glyceric acid in the urine; a primary metabolic error due to deficiency of d-glyceric dehydrogenase resulting in excretion of l-glyceric and oxalic acids, leading to the clinical syndrome of oxalosis with frequent formation of oxalate renal calculi. (05 Mar 2000) |
| acidic amino acid | An Amino acid with a second acid moiety, e.g., glutamic acid, aspartic acid, cysteic acid. (05 Mar 2000) |
| activated amino acid | The product formed by the condensation of the acyl radical of an amino acid and adenosine 5'-monophosphate (originally in the form of adenosine 5'-triphosphate, with elimination of a pyrophosphoric group). Formed in the first step of protein biosynthesis. Synonym: activated amino acid. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|