A cancer drug called hydroxyurea (Droxia, Hydrea) also is used to treat sickle cell anemia.
羟基脲是一种抗肿瘤药，也可以用来治疗镰状细胞性贫血。
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。
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。
This is sickle cell anemia in sickle cell crisis.
出现镰状细胞危象的镰状细胞贫血。
Are patients with sickle cell disease at greater risk of infection?
镰状细胞病患者是否有更高的感染机会？
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。
Hemoglobinopathies such as thalassemias and sickle cell anemia, important genetic diseases of people, have not been seen in other animals.
人的重大遗传性血红蛋白病：例如地中海贫血和镰状细胞性贫血，没有在其它动物中发现。
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。
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。
He was a writer who worked hard for $150 a week. He never whined or complained about money or that he was born with a painful disease called sickle cell.
他写作为生，为了每周150美元的收入辛勤工作，但他从不抱怨钱的问题，也没有因为生来就患有镰刀细胞病——一种伴随着巨大的疼痛的疾病——而自怨自艾。
Scientists have taken a potentially important step toward a therapy for sickle cell disease, a common genetic disorder characterized by malformed red blood cells.
科学家可能已经取得了镰状贫血病治疗技术的一项重大进步。镰状贫血病是一种造成血细胞畸形的常见遗传病。
Scientists have taken a potentially important step toward a therapy for sickle cell disease a common genetic disorder characterized by malformed red blood cells.
科学家可能已经取得了镰状贫血病治疗技术的一项重大进步。镰状贫血病是一种造成血细胞畸形的常见遗传病。
But CRISPR is very real, with the potential, one day, to cure genetically-linked diseases like sickle cell anemia, produce better crops, and create a huge supply of organs for transplant.
不过，CRISPR这种基因编辑技术可是货真价实的。它有可能在未来的某一天治愈细胞性贫血等与基因相关的疾病，种出更好的庄稼，或者带来大量可供移植的器官。
It is also needed for regular transfusions for people with conditions such as thalassaemia and sickle cell disease and is used to make products such as clotting factors for people with haemophilia.
地中海贫血和镰状细胞病等病症患者还需要定期输血，并且血液被用于制造各种制品，例如供血友病患者使用的凝血因子。
If you have a family history of an inherited anemia, such as sickle cell anemia, talk to your doctor and possibly a genetic counselor about your risk and what risks you may pass on to your children.
如果你有贫血家族史，请考虑基因学咨询——关于你患贫血的风险，以及传给下一代的可能性。
Approximately 5% of the world's population carries trait genes for haemoglobin disorders, mainly, sickle-cell disease and thalassaemia.
世界人口近5%携带血红蛋白疾患的特征基因，血红蛋白疾患主要包括镰状细胞病和地中海贫血。
West Africans, and people of West African descent, are susceptible to a disease called sickle-cell anaemia that is virtually unknown elsewhere.
如西非人以及他们的后代易患一种叫做镰状细胞性贫血的疾病，这种病在西非之外几乎都没人听说过。
Sickle-cell anaemia is passed on through a recessive gene.
镰状细胞贫血通过隐性基因遗传给后代。
This condition leads to shortened red blood cell survival, and subsequent anaemia, often called sickle-cell anaemia.
这一状况导致红血球存活期缩短，继而发生贫血，通常称之为镰状细胞贫血。
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。
Poor blood oxygen levels and blood vessel blockages in people with sickle-cell disease can lead to chronic acute pain syndromes, severe bacterial infections, and necrosis (tissue death).
镰状细胞病患者血液含氧量低并且发生血管堵塞，可导致出现慢性和急性疼痛综合症、重度细菌感染和坏疽(组织坏死)。
Sickle-cell disease is characterized by a modification in the shape of the red blood cell from a smooth, donut-shape into a crescent or half moon shape.
镰状细胞病的特征是红血球形状发生突变，由平滑的圆圈形状改变为新月形或半月形。
Or blood cells may be examined for signs of sickle-cell anemia, leukemia, or other disorders.
或检测血液细胞是否有镰状细胞性贫血，白血病或其他疾病的迹象。
Sickle-cell anemia is one of the most prevalent hereditary disorders with prominent morbidity and mortality.
镰状细胞性贫血是最流行的遗传性疾病之一，具有很高的发病率和死亡率。
Sickle-cell anemia is one of the most prevalent hereditary disorders with prominent morbidity and mortality.
镰状细胞性贫血是最流行的遗传性疾病之一，具有很高的发病率和死亡率。
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