thalassaemia的意思
thalassaemia中文翻譯:
n.地中海貧血
thalassemia E───地中海貧血
Recently, gene therapy has been successfully applied to a patient with thalassaemia.───最近,對一名地中海貧血患者成功地應用了基因療法。
Alpha and beta thalassaemia have both mild and severe forms.───alpha型和beta型地中海貧血有輕度和重度兩種形式。
Approximately 5% of the world's population are healthy carriers of a gene for sickle-cell disease or thalassaemia.───全世界近5%的健康人口攜帶有鐮狀細胞病或地中海貧血的基因。
NOTE: Anaemia is not always caused by iron deficiency - lead poisoning and thalassaemia can also produce anaemia.───注意:貧血并不總是由缺鐵引起,鉛中毒和地中海貧血癥也會導致貧血。
This showed that children with homozygous alpha thalassaemia have to lose more red blood cells than their normal counterparts to get SMA.───模型顯示患有純合型alpha型地中海貧血癥的兒童需要失去比正常兒童更多的紅細胞才能患上急性瘧疾性貧血。
Thalassaemia major requires regular blood transfusions to maintain an adequate supply of haemoglobin and sustain life.───重型地中海貧血需要定期輸血,以保持足夠的血紅蛋白供應并維持生命。
There are two major types of thalassaemia, alpha and beta, which are named for the two protein chains that make up normal haemoglobin.───地中海貧血主要分為兩種,即alpha型和beta型,以組成正常血紅蛋白的兩條蛋白鏈命名。
They then modelled the effect a malaria attack would have on both normal children and children with alpha thalassaemia.───然后他們對瘧疾攻擊正常兒童和患有alpha型地中海貧血癥的兒童的效果建立了模型。
Thalassaemia major requires regular blood transfusions to maintain an adequate supply of haemoglobin and sustain life.
Alpha thalassaemia may keep children above that danger level in the face of a malarial attack," she told SciDev.Net.
Alpha thalassaemia, an inherited condition, is common in many areas of the world where malaria is endemic, particularly Africa and southeast Asia.
Sickle-cell disease and severe forms of thalassaemia (thalassaemia major) can occur only when both parents are carriers of trait genes for the particular condition.
The Continuing Education Program aims to help financing thalassaemia major patients with learning aspirations to pursue continuing education and training courses.
A link between alpha thalassaemia and protection from malaria, particularly severe malarial anaemia (SMA), was made in the 1990s.
There are two major types of thalassaemia, alpha and beta, which are named for the two protein chains that make up normal haemoglobin.
People with sickle cell anaemia and thalassaemia are known to have red cells with defects in their outer membranes.
Alpha and beta thalassaemia have both mild and severe forms.
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