| 영문 | uric acid | 한글 | 요산 |
|---|---|---|---|
| 설명 | 결정성의 산. 2, 6, 8-trioxypurine. 화학식은 C5H4N4O3로 사람과 동물의 오줌에서 얻을 수 있다. 핵의 대사산물의 하나. 물, 알콜, 에테르(ether)에는 거의 녹지 않으나 알칼리염의 용액에는 녹는다. 이것의 나트륨염 형태(sodium urate)가 결석의 대부분을 차지한다. 급성백혈병 치료 초기단계와 통풍(Gout)에서 혈중요산이 급격히 오를 수 있다. |
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| 영문 | diabetic nephropathy | 한글 | 당뇨병콩팥병증 |
|---|---|---|---|
| 설명 | 오래된 당뇨의 합병증으로 발생한다. 대개 당뇨병에 이환된 경우 당뇨병 자체에 의한 질병보다 오랜 기간후의 합병증에 의해 목숨을 잃는 경우가 많다. 초기에 당뇨병에서 혈중 포도당농도를 잘 조절한 경우 이런 합병증이 발생하는 경우가 낮으나, 그렇지 못한 경우 신장의 합병증이 발생할 수 있다. 한번 발생한 경우, 치료는 불가능하며, 그 진행 또한 늦출 수 없다. 치료법은 오직 하나 콩팥이식술에 의해서만 가능하며 이식술을 시행한 이후에도 혈당량의 조절은 필수적이다. |
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| 영문 | deoxyribonucleic acid (DNA) | 한글 | 데옥시리보핵산 |
|---|---|---|---|
| 설명 | 핵산의 일종으로 DNA라고도 한다. Deoxyribonucleotide의 중합체이며 유전자의 화학적 본체이다. RNA바이러스 이외의 모든 생물은 DNA를 유전자로 지니고 있다. 디옥시리보뉴클레오티드(deoxyribonucleotide)는 염기와 당(2'-deoxy-D-ribose)과 인산으로 이루어진다. 염기는 아데닌(adenine), 구아닌(guanine), 티민(thymine)및 시토신(cytosine)의 4가지이며, 이것은 당에 부착되어 있다. 인산 역시 당의 한 부분에 부착되어 있다. 이 deoxyribonucleotide의 당은 다른 deoxy- ribonucleotide의 당과 인산을 사이에 놓고 결합을 하게 되어 하나의 긴 사슬을 형성하게 된다. 즉 당과 인산이 주축이 되어서 deoxyribonucleotide의 긴 사슬을 만든다. 이 deoxyribonucleotide의 사슬 두 개는 각각 deoxyribonucleotide에 부착되어 있는 염기들이 결합을 하여 두 개의 사슬이 결합되어 있는 이중나선 구조를 만들게 된다. 4가지 염기 아데닌은 티민과 결합을 하고, 시토신과 결합을 하게 된다. 즉 당과 인산은 긴 사슬을 만드는 역할을 하고 긴 사슬에 부착된 염기들의 결합에 의해서 두 개의 긴 사슬은 서로 붙어서 이중나선 구조를 만든다. DNA의 유전정보는 염기에 저장된다. 4개의 염기의 조합과 배열이 유전정보를 보관하는 하나의 암호 역할을 행하게 된다. |
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| 영문 | retinoic acid | 한글 | 레티노산 |
|---|---|---|---|
| 설명 | C20H28O2. 비타민 A의 알코올기를 알데히드로 산화한 후 다시 카르복실산으로 산화하여 얻은 산. 발생중의 세포에 작용하여 형태를 만드는데 관여한다. |
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| 영문 | ribonucleic acid | 한글 | 리보핵산 |
|---|---|---|---|
| 설명 | Ribonucleotide monomer로 이루어진 핵산으로 염기, 당, 인산으로 구성된다. 염기는 adenine, guanine, cytosine, uracil의 4종류가 있으며, 당은 5탄당이다. RNA는 DNA를 주형으로 하여 상보적으로 결합, 형성되며 단백질을 만들어내는 데에 있어 중요한 역할을 한다. 전령 RNA(mRNA)는 단백질 합성에 있어 가장 기본이 되는 DNA의 서열을 상보적으로 옮겨 받아 전달하는 전령구실을 하는 RNA. 리보솜 RNA(rRNA) 리보솜을 형성하는 4가지 RNA사슬(28S, 18S, 5.8S, 5S로 구성). 전달 RNA(tRNA) 특정 아미노산을 한쪽 끝에 지니고 상보적 서열의 mRNA와 일시적 결합을 이루며 단백질 합성에 직접 기여하는 RNA이다. |
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| AAN | AIDS-associated nephropathy; alpha-amino nitrogen; American Academy of Neurology; American Academy o... |
|---|---|
| UA | absorption unsharpness; ultra-audible; ultrasonic arteriography; umbilical artery; unauthorized abse... |
| BUA | blood uric acid; broadband ultrasonic attenuation |
| SUA | serum uric acid; single umbilical artery; single unit activity |
| U/A | urinalysis; uric acid |
| 1-MU | 1-methyl uric acid |
|---|---|
| FEua | Fractional excretion of uric acid |
| SUA | Serum Uric Acid |
| UA | Uric Acid |
| AN | Analgesic nephropathy |
| uric acid | <biochemistry> The final product of nitrogenous excretion in animals that require to conserve water, such as terrestrial insects or have limited storage space, such as birds and their eggs. Uric acid has very low water solubility and crystals may be deposited in, for example: butterflies wings to impart irridescence. Uric acid, a crystalline body, present in small quantity in the urine of man and most mammals. Combined in the form of urate of ammonia, it is the chief constituent of the urine of birds and reptiles, forming the white part. Traces of it are also found in the various organs of the body. It is likewise a common constituent, either as the free acid or as a urate, of urinary or renal calculi and of the so-called gouty concretions. From acid urines, uric acid is frequently deposited, on standing in a cool place, in the form of a reddish yellow sediment, nearly always crystalline. Chemically, it is composed of carbon, hydrogen, nitrogen, and oxygen, and by decomposition yields urea, among other products. It can be made synthetically by heating together urea and glycocoll. It was formerly called also lithic acid, in allusion to its occurrence in stone, or calculus. See: tophus. Structure: C5H4N4O3 Source: Websters Dictionary (18 Nov 1997) |
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| uric acid infarct | <nephrology, paediatrics> Precipitates of uric acid distending renal collecting tubules in the newborn; since there is no necrosis, the term infarct is a misnomer. (20 Jun 2000) |
| uric acid oxidase | <enzyme> An enzyme that catalyses the conversion of urate and unidentified products. It is a copper protein. The initial products decompose to form allantoin. Chemical name: Urate:oxygen oxidoreductase Registry number: EC 1.7.3.3 (12 Dec 1998) |
| uric | <nephrology> Of or pertaining to urine, obtained from urine. For example; uric acid. Origin: G. Ouron, urine (20 Jun 2000) |
| aids-associated nephropathy | Renal syndrome in human immunodeficiency virus-infected patients characterised by nephrotic syndrome, severe proteinuria, focal and segmental glomerulosclerosis with distinctive tubular and interstitial changes, enlarged kidneys, and peculiar tubuloreticular structures. The syndrome is distinct from heroin-associated nephropathy as well as other forms of kidney disease seen in HIV-infected patients. (12 Dec 1998) |
| analgesic nephropathy | <nephrology, pathology> A form of kidney damage which can occur from the overexposure to certain analgesics (for example acetaminophen, salicylates and non-steroidal anti-inflammatory agents). In most cases analgesic use is excessive in dosing or chronicity of use. Complications include acute renal failure. See: interstitial nephritis. Origin: Gr. Pathos = disease (27 Sep 1997) |
| balkan nephropathy | A tubulointerstitial disease of unknown aetiology occurring in a limited geographic area including adjacent regions of romania, bulgaria, and yugoslavia. (12 Dec 1998) |
| reflux nephropathy | <nephrology> A condition where the chronic backup of urine into a kidney results in kidney damage. Urine is forced out of the bladder and back toward kidney. This condition occurs most commonly in children who have congenital abnormalities of the urinary tract. Symptoms include back pain, flank, pain, abdominal pain, urinary frequency or urgency and blood in the urine. Other symptoms include nausea, fever and chills, most often indicating a kidney infection has occurred. Diagnosis is frequently confirmed by voiding cystourethrogram. Surgery is often required to correct the reflux of urine. Origin: Gr. Pathos = disease (27 Sep 1997) |
| membranous nephropathy | <pathology> A kidney disease that occurs due to inflammation of the kidney glomerulus and its basement membrane. The exact cause is unknown but it appears to be related to the deposition of immune complexes in the basement membrane leading to thickening of the capillary walls. This disorder is a common cause of nephrotic syndrome an is usually how the disease manifests. Risk factors include primary renal disease, malaria, hepatitis B, lupus, syphilis, cancers and non-Hodgkin's lymphomas. Risks also include exposure to some medications such as gold compounds and penicillamine. Mercury, trimethadione and some skin-lightening creams have also been implicated. Treatment includes systemic corticosteroids and immunosuppressive agents. (26 Mar 1998) |
| hereditary deafness and nephropathy | <nephrology, pathology> An inherited disorder involving damage to the kidneys, haematuria and hearing loss. In some individuals vision may also be affected. This genetic disease is uncommon. Symptoms include loss of hearing, abnormal colour to urine, swelling, cough and decline in vision. Inheritance: sex-linked autosomal dominant. Incidence: 1 in 50,000. Origin: Gr. Pathos = disease (27 Sep 1997) |
| hypokalaemic nephropathy | Vacuolation of the epithelial cytoplasm of renal convoluted tubules in patients seriously depleted of potassium; vacuoles do not contain fat or glycogen, concentrating ability is impaired, polyuria and polydipsia are common, and pyelonephritis may develop. Synonym: vacuolar nephrosis. (05 Mar 2000) |
| nephropathy | <nephrology, urology> Any disease of the kidneys. Origin: Gr. Pathos = disease (18 Nov 1997) |
| Danubian endemic familial nephropathy | A tubulointerstitial disease of unknown aetiology occurring in a limited geographic area including adjacent regions of romania, bulgaria, and yugoslavia. (12 Dec 1998) |
| diabetic nephropathy | <nephrology, pathology> Kidney disease and resultant kidney function impairment due to the long standing effects of diabetes on the microvasculature (glomerulus) of the kidney. Features include increased urine protein and declining kidney function. Severe diabetic nephropathy can lead to kidney failure and end-stage renal disease. Origin: Gr. Pathos = disease (27 Sep 1997) |
| IgA nephropathy | <nephrology, pathology> This is a form of glomerulonephritis that results from the deposition of circulating IgA antibody in the kidney tissues. Inflammation of the glomerulus (glomerulonephritis) is the result. This condition may present as acute glomerulonephritis, chronic glomerulonephritis or rapidly progressive glomerulonephritis. Berger's is usually detected in an individual with one or two bouts of bloody urine (usually begins during or soon after a respiratory infection) and no other symptoms of renal disease. Only rarely, will Berger's disease permanently affect kidney function and progress to chronic renal failure. This renal disorder more commonly affects males in the 16-40 age group. Origin: Gr. Pathos = disease (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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