| 영문 | icterus neonatorum | 한글 | 신생아황달 |
|---|---|---|---|
| 설명 | 생후 2일에서 5일되는 갓난아이에게 발생하여 몇 주 후 없어지는 용혈성 황달. 주로 얼굴과 몸통에 나타나며, 오줌이나 똥에는 이상이 없는 생리적인 황달로, 출생 전후에 일어나는 환경 변화에 대한 적응 현상이라고 할 수 있다. |
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| 영문 | icterus, jaundice | 한글 | 황달 |
|---|---|---|---|
| 설명 | 혈액 중에 빌리루빈 양이 증가하여 피부 및 점막내 담즙의 축적으로 황색을 나타내는 병적상태. 빌리루빈은 적혈구에 함유되는 혈색소의 체내에서의 대사산물이며, 간 또는 그 밖의 특수한 세포 속에서 만들어지고 쓸개즙 속에 함유되어 배설되는 적황색 색소이다. 원인은 다음과 같이 셋으로 크게 나눈다. ① 폐색성 황달: 쓸개돌이나 종양 등에 의하여 담관에서 장관으로 유출되어야 할 담즙이 쓸개관의 폐색에 의하여 유출장애를 일으킨 경우. ② 간세포성 황달 및 간세쓸개관성 황달: 간세포의 기능장애에 의한 담즙분비장애를 일으키는 경우로 급성간염에 의하여 대표되는 것. ③ 용혈황달: 과잉의 혈구 파괴로 인하여 일어나는 것으로 주로 용혈성 빈혈인 경우에 일어나는 것이 있다. 또 증세를 경중에 따라 구별하면, 카타르성 황달은 경도의 증세인 경우이며, 두통-권태감 외에 맥박이 느려지고, 때로는 피부가 가려워진다. 중증 황달은 위독한 증세이며, 발열-간부분의 통증, 혼수 등을 볼 수 있고, 급성 간위축증-간경화증-간암 등의 경우에 볼 수 있다. |
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| IC | icteric, icterus; immune complex; immunoconjugate; immunocytochemistry; immunocytotoxicity; impedanc... |
|---|---|
| ICT | icteric, icterus; indirect Coombs test; inflammation of connective tissue; insulin coma therapy; int... |
| Ict | icterus |
| II | icterus index; image intensification or intensifier; Roman numeral two |
| IN | icterus neonatorum; impetigo neonatorum; incidence; incompatibility number; infundibular nucleus; in... |
| FAD | Flavin Adenine Dinucleotide |
|---|---|
| FMN | Flavin mononucleotide |
| FMO | Flavin-containing monooxygenase |
| amine oxidase (flavin-containing) | An oxidoreductase containing flavin and oxidizing amines with the aid of O2 and water to aldehydes or ketones with the release of NH3 and H2O2. Acted upon by antidepressants. Synonym: adrenaline oxidase, diamine oxidase, monoamine oxidase, tyraminase, tyramine oxidase. (05 Mar 2000) |
|---|---|
| chorismate synthase-flavin reductase | <chemical> Bifunctional enzyme from neurospora crassa Synonym: cs-fr enzyme (26 Jun 1999) |
| electron transfer flavin | <biochemistry> Flavoproteins that participate in the electron transport pathway. (05 Mar 2000) |
| flavin | <biochemistry> A derivative of riboflavin (vitamin B2) which can exist as a chemical group of other important biomolecules such as flavin adenine dinucleotide or flavin mononucleotide. (09 Oct 1997) |
| flavin adenine dinucleotide | <biochemistry> Flavin derivatives that act as prosthetic groups (covalently linked cofactors) for flavin enzymes. (18 Nov 1997) |
| flavin-containing monooxygenase-3 | See Fish-odour syndrome. (12 Dec 1998) |
| flavin-linked dehydrogenase | <enzyme> A dehydrogenase that requires a riboflavin coenzyme to function properly. (09 Oct 1997) |
| flavin mononucleotide | <biochemistry> This biomolecule serves as a coenzyme for some enzymes that catalyse oxidation-reduction reactions. (09 Oct 1997) |
| flavin mononucleotide reductase | <enzyme> Nad(p)h + h+ + fmn yields NADP(+) + fmnh(2) Registry number: EC 1.6.99.- Synonym: flavin reductase, fmn reductase, NADPH-fmn oxidoreductase, NADH-fmn oxidoreductase, NADPH-flavin oxidoreductase, NADPH-flavin reductase, NADH-flavin oxidoreductase, frase i (26 Jun 1999) |
| flavin nucleotide | <biochemistry> Flavin derivatives that act as prosthetic groups (covalently linked cofactors) for flavin enzymes. (18 Nov 1997) |
| 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) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| chronic familial 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) |
| physiologic icterus | Icterus which can be accentuated by many factors including excessive haemolysis, sepsis, neonatal hepatitis or congenital atresia of the biliary system. Synonym: physiologic icterus, jaundice of the newborn, neonatal jaundice, physiologic jaundice. (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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|