地中海贫血

Thalassemia is an inherited blood disorder characterized by insufficient production of hemoglobin.
珠蛋白生成障碍性贫血是一种遗传性血液疾病，其特征是血红蛋白生成不足。
A newborn baby was diagnosed with severe thalassemia, requiring immediate medical attention.
一名新生婴儿被诊断出患有严重珠蛋白生成障碍性贫血，需要立即医疗干预。
Genetic testing revealed that the couple were both carriers of thalassemia trait.
遗传检测显示这对夫妇都是珠蛋白生成障碍性贫血携带者。
Regular blood transfusions are necessary for thalassemia patients to maintain a healthy hemoglobin level.
珠蛋白生成障碍性贫血患者需要定期输血以维持正常的血红蛋白水平。
Early detection and treatment can prevent severe complications in children with thalassemia.
对于珠蛋白生成障碍性贫血儿童的早期发现和治疗可以防止严重的并发症。
She underwent a bone marrow transplant to treat her thalassemia, which has significantly improved her health.
她接受了骨髓移植来治疗她的珠蛋白生成障碍性贫血，这极大地改善了她的健康状况。
Education about thalassemia is crucial for pregnant women to make informed decisions about prenatal care.
关于珠蛋白生成障碍性贫血的教育对孕妇了解产前护理至关重要。
The thalassemia support group provides emotional and practical assistance to affected individuals and their families.
珠蛋白生成障碍性贫血支持团体为受影响的个人及其家庭提供情感和实际的帮助。
Doctors are exploring gene therapy as a potential long-term solution for thalassemia.
医生正在探索基因疗法作为治疗珠蛋白生成障碍性贫血的长期解决方案。
Medical advancements have led to better management and improved life expectancy for those living with thalassemia.
医疗进步使得珠蛋白生成障碍性贫血患者的管理得到改善，预期寿命也有所提高。