| 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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| FPR | false-positive rate; finger peripheral resistance; fluorescence photobleaching recovery; N-formylpep... |
|---|---|
| ORSA | osteoclast resorption stimulating activity |
| 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 |
| bone resorption | Bone loss due to osteoclastic activity. (12 Dec 1998) |
|---|---|
| gingival resorption | The exposure of root surface by an apical shift in the position of the gingiva. (12 Dec 1998) |
| resorption | <physiology> The loss of substance through physiologic or pathologic means, such as loss of dentin and cementum of a tooth or of the alveolar process of the mandible or maxilla. Origin: L. Resorbere = to swallow again (10 Mar 1998) |
| resorption atelectasis | The slow partial collapse of a lobe that occurs when communication between alveoli and trachea is obstructed. (05 Mar 2000) |
| resorption lacunae | Tiny depressions, pits, or irregular grooves in bone that is being resorbed by osteoclasts. Synonym: resorption lacunae. (05 Mar 2000) |
| ridge resorption | A loss in the volume and size of the alveolar portion of the mandible or maxilla. (05 Mar 2000) |
| root resorption | Resorption in which cementum or dentin is lost from the root of a tooth owing to cementoclastic or osteoclastic activity in conditions such as trauma of occlusion or neoplasms. (12 Dec 1998) |
| horizontal resorption | A progressive loss of alveolar and supporting bone surrounding the teeth, beginning at the most coronal level of the bone. Synonym: horizontal resorption. (05 Mar 2000) |
| internal resorption | A loss of tooth structure originating within the pulp cavity. (05 Mar 2000) |
| tooth resorption | Resorption of calcified dental tissue, involving demineralization due to reversal of the cation exchange and lacunar resorption by osteoclasts. There are two types: external (as a result of tooth pathology) and internal (apparently initiated by a peculiar inflammatory hyperplasia of the pulp). (12 Dec 1998) |
| embryo resorption | Death and resorption of the embryo that takes place at any developmental stage after ovum implantation and before the completion of organogenesis. does not include foetal resorption. (12 Dec 1998) |
| foetal resorption | <obstetrics> Death and resorption of the foetus at any stage after the completion of organogenesis. It does not include embryo resorption. (12 Dec 1998) |
| 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) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|