| 영문 | secondary infection | 한글 | 이차감염 |
|---|---|---|---|
| 설명 | 어떤 병원체의 감염에 의하여 본인의 저항력이 약해졌을 때 몸의 다른 부위로 전이하여 다시 감염을 일으키는 것. 병원체가 인체에 침입하여 특정한 기관이나 조직에서 병원체가 증식하고, 그곳에 특유의 병터를 일으키는 것이 1차감염 또는 초감염이다. 이 1차감염의 병터의 병원체가 혈관-림프관-기관-소화관-요관 등의 길을 따라 같은 기관의 다른 부위나 다른 기관으로 운반되어 감염을 일으킨다. 따라서 1차감염에 의하여 충분한 면역이 될 경우에는 2차감염이 일어나지 않는다. 예를 들어, 유행성 감기에 걸렸을 때 세균에 의한 폐렴이 뒤따르는 경우를 이른다. 폐렴균, 화농알균, 대장균 따위가 있다. |
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| SA | salicylic acid; saline [solution]; salt added; sarcoidosis; sarcoma; scalenus anticus; secondary ame... |
|---|---|
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| CPSC | congenital paucity of secondary synaptic clefts [syndrome]; Consumer Products Safety Commission |
| HSH | hypomagnesemia with secondary hypocalcemia |
| HSRD | hypertension secondary to renal disease |
| LSIMS | Liquid secondary ion mass spectrometry |
|---|---|
| S | Secondary |
| SIMS | Secondary Ion Mass Spectrometry |
| SLC | Secondary Lymphoid-tissue Chemokine |
| SP | Secondary Polycythaemia |
| secondary methemoglobinaemia | Methemoglobinaemia caused by various chemical agents, such as nitrites. Synonym: enterogenous methemoglobinaemia, secondary methemoglobinaemia. (05 Mar 2000) |
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| acquired methemoglobinaemia | Methemoglobinaemia caused by various chemical agents, such as nitrites. Synonym: enterogenous methemoglobinaemia, secondary methemoglobinaemia. (05 Mar 2000) |
|---|---|
| methemoglobinaemia | The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of haemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinaemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in haemoglobin m (an autosomal dominant trait). (12 Dec 1998) |
| congenital methemoglobinaemia | Methemoglobinaemia due to formation of any one of a group of abnormal a chain or b chain haemoglobins collectively known as haemoglobin M. Slate-gray cyanosis occurs in early infancy, without pulmonary or cardiac disease, and is resistant to ascorbic acid or methylene blue therapy; autosomal dominant inheritance, methemoglobinaemia due to deficiency of cytochrome b5 reductaseor methemoglobin reductase, the enzyme responsible for reduction of intraerythrocyte methemoglobin; cyanosis is improved by ascorbic acid or methylene blue; autosomal recessive inheritance, one case of methemoglobinaemia has been reported that apparently is due to a deficiency of cytochrome b5. Synonym: hereditary methemoglobinaemia, hereditary methemoglobinaemic cyanosis, primary methemoglobinaemia. (05 Mar 2000) |
| primary methemoglobinaemia | Methemoglobinaemia due to formation of any one of a group of abnormal a chain or b chain haemoglobins collectively known as haemoglobin M. Slate-gray cyanosis occurs in early infancy, without pulmonary or cardiac disease, and is resistant to ascorbic acid or methylene blue therapy; autosomal dominant inheritance, methemoglobinaemia due to deficiency of cytochrome b5 reductaseor methemoglobin reductase, the enzyme responsible for reduction of intraerythrocyte methemoglobin; cyanosis is improved by ascorbic acid or methylene blue; autosomal recessive inheritance, one case of methemoglobinaemia has been reported that apparently is due to a deficiency of cytochrome b5. Synonym: hereditary methemoglobinaemia, hereditary methemoglobinaemic cyanosis, primary methemoglobinaemia. (05 Mar 2000) |
| hereditary methemoglobinaemia | Methemoglobinaemia due to formation of any one of a group of abnormal a chain or b chain haemoglobins collectively known as haemoglobin M. Slate-gray cyanosis occurs in early infancy, without pulmonary or cardiac disease, and is resistant to ascorbic acid or methylene blue therapy; autosomal dominant inheritance, methemoglobinaemia due to deficiency of cytochrome b5 reductaseor methemoglobin reductase, the enzyme responsible for reduction of intraerythrocyte methemoglobin; cyanosis is improved by ascorbic acid or methylene blue; autosomal recessive inheritance, one case of methemoglobinaemia has been reported that apparently is due to a deficiency of cytochrome b5. Synonym: hereditary methemoglobinaemia, hereditary methemoglobinaemic cyanosis, primary methemoglobinaemia. (05 Mar 2000) |
| enterogenous methemoglobinaemia | Methemoglobinaemia caused by various chemical agents, such as nitrites. Synonym: enterogenous methemoglobinaemia, secondary methemoglobinaemia. (05 Mar 2000) |
| CS2 secondary alkylsulfohydrolase | <enzyme> From comamonas terrigena Registry number: EC 3.1.6.- Synonym: cs2 sa sulfohydrolase (26 Jun 1999) |
| protein structure, secondary | The stage in the development of protein structure in which regular hydrogen-bond interactions within contiguous stretches of polypeptide chain give rise to alpha helices and beta sheets. This is the first folding level of protein building. (12 Dec 1998) |
| secondary | Second or inferior in order of time, place or importance, derived from or consequent to a primary event or thing. Origin: L. Secundarius, secundus = second (18 Nov 1997) |
| secondary abdominal pregnancy | A condition in which the embryo or foetus continues to grow in the abdominal cavity after its expulsion from the fallopian tube or other seat of its primary development. Synonym: abdominocyesis. (05 Mar 2000) |
| secondary adhesion | Delayed closure of two granulating surfaces. Synonym: secondary adhesion, secondary union. (05 Mar 2000) |
| secondary adrenocortical insufficiency | Adrenocortical insufficiency caused by failure of ACTH secretion resulting from anterior pituitary disease or inhibition of ACTH production resulting from exogenous steroid therapy. (05 Mar 2000) |
| secondary aerodontalgia | Pain referred to the dental area from an area of aerosinusitis. (05 Mar 2000) |
| secondary agammaglobulinaemia | Immunodeficiency in which there is no evident defect in the lymphoid tissues, but rather hypercatabolism or loss of immunoglobulins such as occurs in familial idiopathic hypercatabolic hypoproteinaemia or in defects associated with the nephrotic syndrome. Synonym: secondary agammaglobulinaemia, secondary antibody deficiency, secondary hypogammaglobulinaemia. (05 Mar 2000) |
| secondary alcohol | An alcohol characterised by the bivalent atom group (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|