| 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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| UD | ulcerative dermatosis; ulnar deviation; undetermined; underdeveloped; unit dose; urethral dilatation... |
|---|---|
| UROD | uroporphyrinogen decarboxylase |
| ODC | oritidine decarboxylase; ornithine decarboxylase; oxygen dissociation curve |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| AAD | acute agitated delirium; alloxazine adenine dinucleotide; alpha-1-antitrypsin deficiency; American A... |
| URO-D | Uroporphyrinogen decarboxylase |
|---|---|
| URO-III-S | uroporphyrinogen III synthase |
| AADC | 1-amino acid decarboxylase |
| HD | 1-histidine decarboxylase |
| GAD | Anti-glutamic acid decarboxylase |
| uroporphyrinogen decarboxylase | <enzyme> One of the enzymes active in haem biosynthesis. It catalyses the decarboxylation of uroporphyrinogen III to coproporphyrinogen III by the conversion of four acetic acid groups to four methyl groups. Chemical name: Uroporphyrinogen-III carboxy-lyase Registry number: EC 4.1.1.37 (12 Dec 1998) |
|---|---|
| uroporphyrinogen | See: porphyrinogens. Uroporphyrinogen decarboxylase, an enzyme that participates in haem biosynthesis; it catalyses the decarboxylation of uroporphyrinogen III to produce coproporphyrinogen III; it also acts on uroporphyrinogen I; a deficiency of this enzyme will result in either porphyria cutanea tarda or hepatoerythropoietic porphyria. Uroporphyrinogen III cosynthase, an enzyme in haem biosynthesis that participates in the formation of uroporphyrinogen III; a deficiency of this protein results in congenital erythropoietic porphyria. (05 Mar 2000) |
| uroporphyrinogen-III synthase | <enzyme> An enzyme that catalyses the cyclization of hydroxymethylbilane to yield uroporphyrinogen III and water. Chemical name: Hydroxymethylbilane hydro-lyase (cyclizing) Registry number: EC 4.2.1.75 (12 Dec 1998) |
| uroporphyrinogen I synthetase | <enzyme> An enzyme of haem biosynthesis that is defective in the inherited (autosomal dominant) disease, acute intermittent porphyria. UP I is isomerised to UP III by UP III synthetase, defective in the autosomal recessive disease, congenital erythropoietic porphyria. (18 Nov 1997) |
| adenosylmethionine decarboxylase | <enzyme> An enzyme that catalyses the decarboxylation of s-adenosyl-l-methionine to yield 5'-deoxy-(5'-),3-aminopropyl-(1), methylsulfonium salt. It is one of the enzymes responsible for the synthesis of spermidine from putrescine. Chemical name: S-Adenosyl-L-methionine carboxy-lyase Registry number: EC 4.1.1.50 (12 Dec 1998) |
| alpha-ketoarginine decarboxylase | <enzyme> Alpha-ketoarginine gives gamma-guanidinobutyraldehyde Registry number: EC 4.1.1.- Synonym: alpha keto-arginine decarboxylase (26 Jun 1999) |
| aromatic d-amino-acid decarboxylase | <enzyme> An enzyme that catalyses the decarboxylation of l-dopa to dopamine, of l-tryptophan to tryptamine, and of l-hydroxytryptophan to serotonin; important in the biosynthetic pathway of catecholamines and melanin. Synonym: dopa decarboxylase, hydroxytryptophan decarboxylase, tryptophan decarboxylase. (05 Mar 2000) |
| aspartate 1-decarboxylase | <enzyme> A pyridoxal-phosphate protein that catalyses the alpha-decarboxylation of l-glutamic acid to form gamma-aminobutyric acid and carbon dioxide. The enzyme is found in bacteria and in invertebrate and vertebrate nervous systems. It is the rate-limiting enzyme in determining gaba levels in normal nervous tissues. The brain enzyme also acts on l-cysteate, l-cysteine sulfinate, and l-aspartate. Chemical name: L-Glutamate-1-carboxy-lyase Registry number: EC 4.1.1.15 (12 Dec 1998) |
| aspartate 4-decarboxylase | Aspartate beta-decarboxylase;a carboxy-lyase converting l-aspartate to l-alanine (releasing CO2); it decarboxylates aminomalonate and (in bacteria) removes SO2 from cysteinesulfinate. See: desulfinase. (05 Mar 2000) |
| aspartate-alpha-decarboxylase | <enzyme> Forms beta-alanine Registry number: EC 4.1.1.11 Synonym: aspartate 1-decarboxylase (26 Jun 1999) |
| carboxynorspermidine decarboxylase | <enzyme> Nspc protein isolated from vibrio alginolyticus; genbank d31783 Registry number: EC 4.1.1.- Synonym: cans dc, nspc gene product (26 Jun 1999) |
| malonate saemialdehyde decarboxylase | <enzyme> Forms acetaldehyde and carbon dioxide Registry number: EC 4.1.1.- (26 Jun 1999) |
| glutaconyl CoA decarboxylase | <enzyme> Forms crotonyl CoA Registry number: EC 4.1.1.- Synonym: glutaconyl coenzyme a decarboxylase (26 Jun 1999) |
| glutamate decarboxylase | <enzyme> A pyridoxal-phosphate protein that catalyses the alpha-decarboxylation of l-glutamic acid to form gamma-aminobutyric acid and carbon dioxide. The enzyme is found in bacteria and in invertebrate and vertebrate nervous systems. It is the rate-limiting enzyme in determining gaba levels in normal nervous tissues. The brain enzyme also acts on l-cysteate, l-cysteine sulfinate, and l-aspartate. Chemical name: L-Glutamate-1-carboxy-lyase Registry number: EC 4.1.1.15 (12 Dec 1998) |
| methionine decarboxylase | <enzyme> From fern dryopteris filix-mas; pyridoxal 5'-phosphate required for activity; converts methionine to 3-(methylthio)propionaldehyde Registry number: EC 4.1.1.57 Synonym: l-methionine decarboxylase (26 Jun 1999) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|