| 영문 | thalassemia | 한글 | 지중해빈혈 |
|---|---|---|---|
| 설명 | 혈색소의 합성에 장애가 있는 다양한 종류의 선천병으로서 한국을 비롯한 동양권에는 매우 드물다. 혈색소 장애에 의하여 작은적혈구성, 저염색성 빈혈(정상 크기보다 작은 적혈구 크기와 정상보다 적은 염색이 일어난다)이 유발됨. 크게 헤모글로빈의 알파사슬에 이상이 있는 α-thalassemia와 베타사슬에 이상이 있는 β-thalassemia로 구분된다. 치료는 빈혈이 심한 경우 수혈을 해주어야 하며, 특별한 치료는 없다. |
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| ATR | Achilles tendon reflex; alpha-thalassemia-mental retardation [syndrome] |
|---|---|
| ATRX, ATR-X | X-linked alpha-thalassemia mental retardation [syndrome] |
| S/b | sickle cell beta-thalassemia |
| ST | esotropia; scala tympani; scaphotrapezoid; sclerotherapy; sedimentation time; semitendinosus; sensor... |
| S-T | [segment] in electrocardiography, the portion of the segment between the end of the S wave and the b... |
| TM | Beta-thalassemia major |
|---|---|
| TI | Thalassemia Intermedia |
| TM | Thalassemia Major |
| haemoglobin Anti-Lepore | A group of abnormal haemoglobins similar to haemoglobin Lepore. These haemoglobins have normal a chains, but the non-a chain consists of the N-terminal portion of the b chain joined to the C-terminal portion of the d chain. This is the opposite crossing over pattern observed in haemoglobin Lepore. Examples of haemoglobin Anti-Lepore include HbMiyada, Hb PCongo, Hb PNilotic, and HbLincoln Park. There is also one variant that is both haemoglobin Lepore and haemoglobin Anti-Lepore (HbParchman). Compare: haemoglobin Lepore. (05 Mar 2000) |
|---|---|
| haemoglobin Lepore | A group of abnormal Hb's with normal a chains, but the non-a chains consist of the N-terminal portion of the d chain joined to the C-terminal portion of the b chain, apparently as the result of nonhomologous pairing and crossing over between the genes for b and d chains. The major types are Hb LeporeBoston (identical to Hb LeporeWashington), Hb LeporeHollandia, and Hb LeporeBaltimore, which differ in the region of crossing over (d87-b116, d22-b50, and d50-b86, respectively). Heterozygotes form about 10% Hb Lepore, normal amounts of Hb A2, and moderately increased amounts of Hb F and usually have mild anaemia, microcytosis, and hypochromia; homozygotes form only Hb Lepore and Hb F and have severe anaemia. Compare: haemoglobin Anti-Lepore. (05 Mar 2000) |
| Lepore haemoglobin | <haematology> Variant haemoglobin in a rare form of thalassaemia: there is a composite _ _ chain as a result of an unequal crossing over event. The composite chain is functional but synthesised at reduced rate. (18 Nov 1997) |
| Lepore thalassaemia | Thalassaemia syndrome due to production of abnormally structured Lepore haemoglobin. Heterozygous state: thalassaemia minor with about 10% of Hb Lepore, Hb F moderately increased, Hb A2 normal. Homozygous state: thalassaemia major with only Hb F and Hb Lepore produced, no Hb A or Hb A2. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|