| 영문 | iron deficiency anemia | 한글 | 철결핍빈혈 |
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| 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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| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
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| DBH | Dopamine-Beta(β)-Hydroxylase |
| AHH | alpha-hydrazine analog of histidine; anosmia and hypogonadotropic hypogonadism [syndrome]; arylhydro... |
| DBH | dopamine beta-hydroxylase |
| PPH | past pertinent history; persistent pulmonary hypertension; phosphopyruvate hydratase; postpartum hem... |
| PAH | Phenylalanine hydroxylase |
|---|---|
| PH | Phenylalanine hydroxylase |
| D-Phe | D-Phenylalanine |
| Phe | D-phenylalanine |
| FMLP | Formyl methionyl leucyl phenylalanine |
| phenylalanine 4-hydroxylase | <enzyme> An enzyme that catalyses the oxidation of l-phenylalanine to l-tyrosine with O2 and tetrahydrobiopterin (the latter forming the dihydro derivative) which is reduced by NADPH and a reductase to the active form; a deficiency of either of these enzymes will result in phenylketonuria. Synonym: phenylalanine 4-hydroxylase. (05 Mar 2000) |
|---|---|
| phenylalanine hydroxylase | <enzyme> An enzyme of the oxidoreductase class that catalyses the reaction l-phenylalanine, tetrahydrobiopterin, and oxygen to yield l-tyrosine, dihydrobiopterin, and water, the reaction synthesizing tyrosine from phenylalanine. Chemical name: L-Phenylalanine,tetrahydrobiopterin:oxygen oxidoreductase (4-hydroxylating) Registry number: EC 1.14.16.1 (12 Dec 1998) |
| phenylalanine hydroxylase phosphatase | <enzyme> Catalyses dephosphorylation of phosphorylated phenylalanine hydroxylase Registry number: EC 3.1.3.- Synonym: phe hydroxylase phosphatase (26 Jun 1999) |
| 17-hydroxylase deficiency syndrome | <syndrome> Congenital deficiency of adrenocortical, and possibly ovarian, steroid C-17a hydroxylase; the resulting excessive secretion of corticosterone and deoxycorticosterone produces hypertension and hypokalaemic alkalosis; absence of aldosterone secretion in such patients may indicate a multiple enzymic deficiency. (05 Mar 2000) |
| phenylalanine | <amino acid> One of the amino acids which the body cannot manufacture itself, but must acquire from food. It is abundant in meats and cheese. Phenylalanine is a precursor of tyrosine and together they lead to the formation of thyroxine or thyroid hormone and of adrenaline and noradrenaline which is converted into a neurotransmitter, a brain chemical which transmits nerve impulses. This neurotransmitter is used by the brain to manufacture noradrenaline which promotes mental alertness, memory, elevates mood and suppresses the appetite very effectively. Along with another amino acid, tryptophan, phenylalanine governs the release of an intestinal hormone called cholecystokinin. Overuse of phenylalanine supplements can cause anxiety, headaches and hypertension and are contraindicated for pregnant woman, those who suffer from anxiety attacks, high blood pressure, PKU, pigmented melanoma or anyone taking an anti-depressant containing monoamine oxidase inhibitors. (15 Oct 1997) |
| phenylalanine 4-monooxygenase | <enzyme> An enzyme that catalyses the oxidation of l-phenylalanine to l-tyrosine with O2 and tetrahydrobiopterin (the latter forming the dihydro derivative) which is reduced by NADPH and a reductase to the active form; a deficiency of either of these enzymes will result in phenylketonuria. Synonym: phenylalanine 4-hydroxylase. (05 Mar 2000) |
| phenylalanine aminopeptidase | <enzyme> Metalloenzyme from legionella pneumophila; mw: 35,000; pH optimum 8-9.5 Registry number: EC 3.4.11.- (26 Jun 1999) |
| phenylalanine ammonia lyase | <enzyme> An enzyme that catalyses the deamination of l-phenylalanine to form trans-cinnamate and ammonia. It may also act on l-tyrosine. Since the enzyme deprives neoplastic tissue of phenylalanine, it has been used experimentally in the treatment of acute lymphoblastic leukaemia. The enzyme is obtained from many plants and is used as an enzymic marker for lignification and other developmental processes in plant cells. Pharmacological action: antineoplastic agent. Chemical name: L-Phenylalanine ammonia-lyase Registry number: EC 4.3.1.5 (12 Dec 1998) |
| phenylalanine oxidase | <enzyme> Forms phenylpyruvate in the presence of air; consider also phenylalanine dehydrogenase (nad) which requires nad Registry number: EC 1.4.3.- Synonym: phenylalanine desaminase, l-phenylalanine oxidase, phenylalanine dehydrogenase (26 Jun 1999) |
| phenylalanine-trna ligase | <enzyme> An enzyme that activates phenylalanine with its specific transfer RNA. Chemical name: Phenylalanine:tRNA(Phe) ligase (AMP-forming) Registry number: EC 6.1.1.20 (12 Dec 1998) |
| n-formylmethionine leucyl-phenylalanine | <chemical> N-formylmethionyl-leucyl-phenylalanine. A formylated tripeptide originally isolated from bacterial filtrates that is positively chemotactic to polymorphonuclear leucocytes, and causes them to release lysosomal enzymes and become metabolically activated. Chemical name: L-Phenylalanine, N-(N-(N-formyl-L-methionyl)-L-leucyl)- (12 Dec 1998) |
| N-formylmethionyl-leucyl-phenylalanine carboxypeptidase | <enzyme> Human salivary enzyme liberates phenylalanine from the chemotactic peptide n-formylmethionine leucyl-phenylalanine Registry number: EC 3.4.- Synonym: n-formyl-methionine leucyl-phenylalanyl carboxypeptidase, formylmet-leu-phe carboxypeptidase (26 Jun 1999) |
| abscisic acid 8'-hydroxylase | <enzyme> Catalyses conversion of abscisic acid to 8'-hydroxyabscisic acid, which rearranges to phaseic acid Registry number: EC 1.14.99.- Synonym: aba 8'-hydroxylase (26 Jun 1999) |
| aflatoxin B1 hydroxylase | <enzyme> Hydroxylases may be replaced by mixed function oxidases as appropriate Registry number: EC 1.14.- Synonym: aflatoxin b1 4-hydroxylase (26 Jun 1999) |
| aklavinone 11-hydroxylase | <enzyme> A flavin-type bacterial hydroxylase from streptomyces peucetius; 489 amino acid residues, mw 52.3 kD; genbank u09844 Registry number: EC 1.14.14.- Synonym: dnrf protein, dnrf gene product (26 Jun 1999) |
| phenylalanine hydroxylase deficiency |
phenylketonuria.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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