thalassaemia

thalassaemia

美 　英

• 网络地中海贫血；地中海贫血病；地中海贫血症

英汉解释

n.	1. a hereditary form of anaemia, particularly prevalent around the Mediterranean, that is caused by a dysfunction in the synthesis of the red blood pigment haemoglobin

例句

NOTE: Anaemia is not always caused by iron deficiency - lead poisoning and thalassaemia can also produce anaemia.

注意：贫血并不总是由缺铁引起，铅中毒和地中海贫血症也会导致贫血。

This showed that children with homozygous alpha thalassaemia have to lose more red blood cells than their normal counterparts to get SMA.

模型显示患有纯合型alpha型地中海贫血症的儿童需要失去比正常儿童更多的红细胞才能患上急性疟疾性贫血。

Approximately 5% of the world's population are healthy carriers of a gene for sickle-cell disease or thalassaemia.

全世界近5%的健康人口携带有镰状细胞病或地中海贫血的基因。

Thalassaemia major requires regular blood transfusions to maintain an adequate supply of haemoglobin and sustain life.

重型地中海贫血需要定期输血，以保持足够的血红蛋白供应并维持生命。

There are two major types of thalassaemia, alpha and beta, which are named for the two protein chains that make up normal haemoglobin.

地中海贫血主要分为两种，即alpha型和beta型，以组成正常血红蛋白的两条蛋白链命名。

They then modelled the effect a malaria attack would have on both normal children and children with alpha thalassaemia.

然后他们对疟疾攻击正常儿童和患有alpha型地中海贫血症的儿童的效果建立了模型。

Alpha and beta thalassaemia have both mild and severe forms.

alpha型和beta型地中海贫血有轻度和重度两种形式。

A link between alpha thalassaemia and protection from malaria, particularly severe malarial anaemia (SMA), was made in the 1990s.

在20世纪90年代科学家发现了alpha型地中海贫血症和防御疟疾——特别是防御急性疟疾性贫血（SMA）——之间的联系。

Thalassaemia patients and their families

地中海贫血病患者及其家属

The Thalassaemia Association of Hong Kong

香港地中海型贫血病协会