sickle-cell disease

sickle-cell disease

美 　英

• un.镰刀形红胞病
• 网络镰刀型红血球病变；镰刀型红细胞病；镰形细胞贫血症

英汉解释

un.

1. 镰刀形红胞病

例句

This article describes an audit of pain management in sickle cell disease that was used to generate practice guidelines.

本文介绍了镰状细胞病疼痛的管理审计，这是用来生成实践准则。

Such screening techniques and early intervention therapies have sharply lowered the mortality rate in children with sickle cell disease.

这样的筛选技术和早期介入性治疗显著降低了患镰形细胞贫血症儿童的死亡率。

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。

Patients with sickle cell disease or trait are particularly susceptible to glaucomatous optic nerve damage from even mildly elevated IOPs.

对于患有镰状细胞贫血的患者而言，即使是轻微的IOP升高，也很有可能造成青光眼性视神经损伤。

Babies with sickle cell disease typically do not exhibit symptoms until after 6 months of age.

患有镰形细胞贫血症的婴儿一般在6个月大的时候才会表现出病发症状。

High risk conditions included asthma, sickle cell disease, HIV infection, and chronic cardiac disease, among others.

高风险状态包括：哮喘，镰状红细胞贫血，艾滋病毒感染，慢性心脏疾病，等等。

Transfusions are usually not required nor recommended for standard aso-occlusie crises or pain associated with sickle cell disease.

对于镰状细胞病相关的标准血管阻塞性危象或疼痛，输血治疗常没有必要，且不推荐使用。

Sickle cell disease is a blood disorder due to a single genetic mutation.

镰形细胞（贫血）症是一种血液疾病，是由于某种基因变异引起的。

In other studies, bone marrow transplants cure severe sickle cell disease in almost two hundred children.

在其他研究中，骨髓移植治愈了差不多两百名患有严重镰状细胞（贫血）病的孩子。

Sickle cell disease is a disorder in which blood cells carry a mutation in hemoglobin.

镰状细胞贫血病是由于血细胞携带了一种突变的血红蛋白导致的紊乱。

Millions of people around the world, most of them of African origin, suffer from sickle cell disease.

全球患有镰状贫血病的人们数以百万计，多数为非洲后裔。

To investigate BCL11A's therapeutic value, Orkin's team turned to a mouse model for sickle cell disease.

为了进一步研究BCL11A的治疗价值，奥尔金的研究小组转向镰状贫血症的白鼠模型。

Other researchers are working on gene therapy as another approach to cure sickle cell disease, but progress has been slow.

其他研究者正在钻研基因疗法，这也是镰形细胞贫血症的另一疗法，然而进展很缓慢。

Black people in Africa are the huge majority of those with sickle cell disease.

非洲的黑人是患有镰状细胞（贫血）病的巨大群体。

People with sickle cell disease can suffer severe pain, bacterial infections and the death of tissue.

患有镰状细胞（贫血）病的人将经受巨痛、细菌感染和组织坏死。

Transfusions hae been ealuated to treat certain severe complications of sickle cell disease.

通过输血治疗镰状细胞病的一些严重的并发症。

In addition to infection, stroke was also a leading cause of death in children with sickle cell disease.

除感染外，中风也是导致镰形细胞贫血儿童死亡的主要原因。

People with sickle cell disease have a faulty gene that makes their red blood cells change shape and block small blood vessels.

患有镰状细胞病的人拥有一个缺陷基因，这让他们的红细胞改变形状，阻塞小血管。这会导致疼痛、器官损伤和中风。

Since 2006, newborn screening tests for sickle cell disease have been performed in all 50 states.

从2006年起，新生儿镰形细胞贫血症筛查检验已经在美国所有50个州实行。

The average life span of a person with sickle cell disease is just 42 years for men and 48 years for women.

男性镰状贫血病患者的平均寿命仅为42岁，女性仅为48岁。

What is responsible for the "anemia" of sickle cell disease?

镰状细胞病的“贫血”的原因？

But they also include sickle-cell disease, a blood disorder that is the biggest non-communicable killer of Africa's children.

但廉形红细胞疾病——一种因血液紊乱而导致最多非洲婴儿死亡的非传染性疾病——也是原因之一。

In fact, the lifespan of erythrocytes in sickle cell disease has been observed to be only 10-12 days, compared to the normal 120 days (4).

事实上，据观察，镰状细胞病红细胞的寿命只有10-12天，而正常红细胞的寿命为120天[4]。

Sickle-cell disease can be managed by simple procedures including

镰状细胞病可通过一些简单措施加以管理，包括

Renaissance Of Sickle Cell Disease Research In The Genomic Era

基因时代的镰状细胞疾病研究新生

BMC Cell Biology Sickle Cell Disease Association of America Sickle Cell Society

国际细胞生物学联盟欧洲生命科学学会英国细胞生物学学会美国细胞生物学学会日本色素细胞学会