| 영문 | iron deficiency anemia | 한글 | 철결핍빈혈 |
|---|---|---|---|
| 설명 | 적혈구의 기능은 산소를 운반하는데 있다. 적혈구 속에 산소와 결합을 하여 산소를 운반하는 혈색소라는 물질이 있다. 철은 이 혈색소의 중요한 부분을 이루는 것으로 철이 없으면 혈색소가 만들어질 수가 없다. 혈색소가 없으면 역시 적혈구도 만들어지지 않으므로 체내에 철이 부족하면 빈혈이 생긴다. 이 철결핍성 빈혈은 빈혈의 원인 중에서 가장 흔한 것이다(약 25%를 차지한다). 철저장량의 저하-결핍, 혈청철농도의 저하, 트란스페린량 상승, 트란스페린포화도의 저하, 혈색소농도 또는 헤마토크리트의 저하, 저색소성대적혈구를 특징으로 하는 빈혈로서, 생체 내에서 철이 장기에 걸쳐 결핍되며 그 때문에 혈색소 생산 감소에 의해 일어난다. 창자에서의 철흡수량 부족, 철의 수요 증대(유아기, 사춘기, 임신), 철소실과잉(출혈)에 의해 일어나며, 특히 사춘기에서 폐경기까지의 여성에게 많다. 증상으로서는 얼굴창백, 피로감, 피부창백, 손톱 변화(스푼 모양) 등을 나타낸다. 구강 영역에서는 혀의 접촉통, 발적, 건조감, 삼킴곤란을 수반하면 플러머-빈슨(Plummer-Vinson)증후군이라고 한다. 혈액 소견은 혈청철은 저하하며, 철결합능력의 상승, 저색소성 작은적혈구성을 나타낸다. |
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| PHI | passive hemagglutination inhibition; past history of illness; phosphohexose isomerase; physiological... |
|---|---|
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| IGD | idiopathic growth hormone deficiency; interglobal distance; isolated gonadotropin deficiency |
| MCD | magnetic circular dichroism; mast-cell degranulation; mean cell diameter; mean of consecutive differ... |
| CSCI | corticosterone side-chain isomerase |
| PHI | Phosphohexose isomerase |
|---|---|
| 3 beta-HSD | 3 beta-Hydroxysteroid dehydrogenase/isomerase |
| 3 beta-HSD | 3 beta-Hydroxysteroid dehydrogenasel delta 5-->4-isomerase |
| 3 beta-HSD | 3 beta-hydroxy-steroid dehydrogenase/delta 5-delta 4 isomerase |
| PMI | 6-phosphomannose isomerase |
| phosphohexose isomerase deficiency | <enzyme> An enzyme deficiency characterised by chronic nonspherocytic haemolytic anaemia; autosomal recessive inheritance. Synonym: phosphohexose isomerase deficiency. (05 Mar 2000) |
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| phosphohexose isomerase | <enzyme> An enzyme that catalyses the reversible interconversion of d-fructose 6-phosphate and d-glucose-6-phosphate; a part of glycolysis and gluconeogenesis; glucosephosphate isomerase deficiency is an inherited disorder resulting in liver glycogenesis and haemolytic anaemia. Synonym: hexosephosphate isomerase, phosphohexomutase, phosphohexose isomerase. (05 Mar 2000) |
|---|---|
| glucosephosphate isomerase deficiency | <enzyme> An enzyme deficiency characterised by chronic nonspherocytic haemolytic anaemia; autosomal recessive inheritance. Synonym: phosphohexose isomerase deficiency. (05 Mar 2000) |
| acetylene-allene thioester isomerase | <enzyme> Converts 3-acetylenic fatty acyl thioesters to 2,3-dienoyl fatty acyl thioesters Registry number: EC 5.3.99.- (26 Jun 1999) |
| arabinose-5-phosphate isomerase | <enzyme> Catalyses reversibly the conversion of arabinose phosphate to ribulosephosphate Registry number: EC 5.3.1.13 Synonym: arabinose 5-phosphate ketolisomerase, arabinosephosphate isomerase (26 Jun 1999) |
| galactose-6-phosphate isomerase | <enzyme> Converts galactose 6-phosphate to tagatose 6-phosphate Registry number: EC 5.3.1.- Synonym: galactose 6-phosphate isomerase, gal-6-p isomerase, tagatose-6-phosphate isomerase (26 Jun 1999) |
| maleate isomerase | <enzyme> Converts maleate to fumarate; amino acid sequence sourced from from alcaligenes faecalis. Registry number: EC 5.2.1.1 Synonym: maleate cis-trans-isomerase (26 Jun 1999) |
| maleylpyruvate isomerase | <enzyme> Catalyses isomerization of 3-maleylpyruvate to 3-fumarylpyruvate Registry number: EC 5.2.1.4 (26 Jun 1999) |
| mannose-6-phosphate isomerase | <enzyme> An enzyme that catalyses the reversible isomerization of d-mannose-6-phosphate to form d-fructose-6-phosphate, an important step in glycolysis. Chemical name: D-Mannose-6-phosphate ketol isomerase Registry number: EC 5.3.1.8 (12 Dec 1998) |
| mannosephosphate isomerase | <enzyme> An enzyme that catalyses the reversible conversion of d-mannose-6-phosphate to d-fructose-6-phosphate; a key step in the synthesis of mannose derivatives as well as the entry of mannose into the central pathways of carbohydrate metabolism. (05 Mar 2000) |
| glucose-6-phosphate isomerase | <enzyme> An enzyme that catalyses the reversible interconversion of glucose-6-phosphate and fructose-6-phosphate, and is a part of the glycolytic and gluconeogenic pathways. Deficiency of the enzyme, an autosomal recessive trait, results in liver glycogenesis and haemolytic anaemia. Chemical name: D-Glucose-6-phosphate ketol-isomerase Registry number: EC 5.3.1.9 (12 Dec 1998) |
| glucose isomerase | <enzyme> An isomerase enzyme which converts the sugar glucose into the sugar fructose. Fructose is a structural isomer of glucose. (09 Oct 1997) |
| glucose-phosphate isomerase | <enzyme> An enzyme that catalyses the reversible interconversion of d-fructose 6-phosphate and d-glucose-6-phosphate; a part of glycolysis and gluconeogenesis; glucosephosphate isomerase deficiency is an inherited disorder resulting in liver glycogenesis and haemolytic anaemia. Synonym: hexosephosphate isomerase, phosphohexomutase, phosphohexose isomerase. (05 Mar 2000) |
| retinaldehyde isomerase | <enzyme> Converts all-trans-retinal to 11-cis-retinal Registry number: EC 5.2.1.3 Synonym: retinal photoisomerase (26 Jun 1999) |
| retinal isomerase | <enzyme> Converts all-trans-retinal to 11-cis-retinal Registry number: EC 5.2.1.3 Synonym: retinal photoisomerase (26 Jun 1999) |
| retinol isomerase | <enzyme> Catalyses the isomerization of all trans-retinol to 11-cis-retinol in the dark; found in the pigment epithelium in the eye Registry number: EC 5.2.1.7 Synonym: retinoid isomerase (26 Jun 1999) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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