| 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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| mAD, MADA | muscle adenylate deaminase; myoadenylate deaminase |
|---|---|
| MAD | major affective disorder; mandibulo-acral dysplasia; maximum allowable dose; methylandrostenediol; m... |
| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
| ADA | adenosine deaminase; American Dental Association; American Dermatological Association; American Diab... |
| ADase | adenosine deaminase |
| ADA | Adenosin deaminase |
|---|---|
| ADA | Adenosine Deaminase activity |
| CD | Cytidine Deaminase |
| CDA | Cytidine deaminase |
| CDD | Cytidine deaminase |
| myoadenylate deaminase | Muscle AMP deaminase. See: AMP deaminase. (05 Mar 2000) |
|---|---|
| adenine deaminase | <enzyme> An enzyme that catalyses the hydrolysis of adenine to ammonia and hypoxanthine. A part of purine degradation. (05 Mar 2000) |
| adenosine deaminase | <enzyme> An enzyme that catalyses the hydrolysis of adenosine to inosine with the elimination of ammonia. Since there are wide tissue and species variations in the enzyme, it has been used as a tool in the study of human and animal genetics and in medical diagnosis. Chemical name: Adenosine aminohydrolase Registry number: EC 3.5.4.4 (12 Dec 1998) |
| adenylic acid deaminase | <enzyme> An enzyme that catalyses the deamination of AMP to imp. Chemical name: AMP aminohydrolase Registry number: EC 3.5.4.6 (12 Dec 1998) |
| AMP deaminase | <enzyme> An enzyme that catalyses the deamination of AMP to imp. Chemical name: AMP aminohydrolase Registry number: EC 3.5.4.6 (12 Dec 1998) |
| blasticidin S deaminase | <enzyme> Catalyses deamination of cytosine moiety of blasticidin s Registry number: EC 3.5.4.23 (26 Jun 1999) |
| guanine deaminase | <enzyme> An enzyme that catalyses the deamination of guanine to form xanthine. Chemical name: Guanine aminohydrolase Registry number: EC 3.5.4.3 (12 Dec 1998) |
| phosphoribosylaminopyrimidine deaminase | <enzyme> Intermediate in riboflavin biosynthesis Chemical name: 2,5-diamino-6-oxy-4-(5'-phosphoribosylamino) pyrimidine deaminase Registry number: EC 3.5.4.- (26 Jun 1999) |
| cytidine deaminase | <enzyme> An enzyme that catalyses the deamination of cytidine, forming uridine. Chemical name: Cytidine aminohydrolase Registry number: EC 3.5.4.5 (12 Dec 1998) |
| S-adenosylhomocysteine deaminase | <enzyme> From streptomyces flocculus; deaminating enzyme responsible for the conversion of s-adenosylhomocysteine to s-inosylhomocysteine Registry number: EC 3.5.4.- Synonym: adohcy deaminase (26 Jun 1999) |
| histidine deaminase | <enzyme> An enzyme of the lyase class that catalyses the reaction of l-histidine to form urocanate and ammonia. The reaction is the initial step of histidine catabolism. Genetic deficiency of the enzyme, transmitted as an autosomal recessive trait, causes histidinaemia. Chemical name: L-Histidine ammonia-lyase Registry number: EC 4.3.1.3 (12 Dec 1998) |
| pterin deaminase | An aminohydrolase catalyzing hydrolytic deamination of 2-amino-4-hydroxypteridine to form 2,4-dihydroxypteridine and ammonia. (05 Mar 2000) |
| homoserine deaminase | <enzyme> A multifunctional pyridoxal phosphate enzyme. In the final step in the biosynthesis of cysteine it catalyses the cleavage of cystathionine to yield cysteine, ammonia, and 2-ketobutyrate. Chemical name: L-Cystathionine cysteine-lyase (deaminating) Registry number: EC 4.4.1.1 (12 Dec 1998) |
| serine deaminase | <enzyme> A pyridoxal-phosphate protein that catalyses the deamination of threonine to 2-ketobutyrate and ammonia. The role of this enzyme can be biosynthetic or biodegradative. In the former role it supplies 2-ketobutyrate required for isoleucine biosynthesis, while in the latter it is only involved in the breakdown of threonine to supply energy. Chemical name: L-Threonine hydro-lyase (deaminating) Registry number: EC 4.2.1.16 (12 Dec 1998) |
| dcmp deaminase | <enzyme> An enzyme that catalyses the hydrolytic deamination of deoxycytidylic acid to deoxyuridylic acid and ammonia. It plays an important role in the regulation of the pool of deoxynucleotides in higher organisms. The enzyme also acts on some 5-substituted deoxycytidylic acids. Chemical name: dCMP aminohydrolase Registry number: EC 3.5.4.12 (12 Dec 1998) |
| myoadenylate deaminase deficiency |
a mild autosomal recessive disorder, due to defective AMP deaminase in the purine nucleotide cycle, and characterized clinically by fatigue, cramps, and myalgia after exercise.
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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