thalassemia major
重型地中海贫血
thalassemia minor
轻型地中海贫血
thalassemia trait
地中海贫血特征
alpha thalassemia
α型地中海贫血
beta thalassemia
β型地中海贫血
thalassemia screening
地中海贫血筛查
thalassemia test
地中海贫血检测
thalassemia carrier
地中海贫血携带者
thalassemia diagnosis
地中海贫血诊断
thalassemia patient
地中海贫血患者
thalassemia is a hereditary blood disorder characterized by abnormal hemoglobin production.
地中海贫血是一种遗传性血液疾病，其特征是血红蛋白生成异常。
many people are unaware they carry the thalassemia gene until their child is diagnosed.
许多人直到孩子被确诊才知道自己携带地中海贫血基因。
regular blood transfusions are essential for patients with thalassemia major.
定期输血对地中海贫血重症患者至关重要。
prenatal screening can detect thalassemia in unborn babies with high accuracy.
产前筛查可以高准确度地检测胎儿是否患有地中海贫血。
iron overload is a serious complication that requires chelation therapy in thalassemia patients.
铁过载是一种严重的并发症，地中海贫血患者需要螯合治疗。
thalassemia carrier screening is recommended for couples planning to start a family.
建议计划组建家庭的夫妇进行地中海贫血携带者筛查。
the severity of thalassemia depends on how many mutated genes a person inherits.
地中海贫血的严重程度取决于一个人继承了多少突变基因。
advances in gene therapy offer new hope for curing thalassemia in the future.
基因治疗的进步为未来治愈地中海贫血带来了新的希望。
thalassemia intermedia patients experience moderate symptoms compared to the major form.
中间型地中海贫血患者的症状比重型患者轻微。
children with thalassemia major often require lifelong medical care and support.
重型地中海贫血儿童通常需要终身的医疗护理和支持。
genetic counseling helps families understand the risks of passing thalassemia to their children.
遗传咨询帮助家庭了解将地中海贫血遗传给孩子的风险。
thalassemia is most prevalent in mediterranean, african, and southeast asian populations.
地中海贫血在地中海、非洲和东南亚人群中最为普遍。
thalassemia major
重型地中海贫血
thalassemia minor
轻型地中海贫血
thalassemia trait
地中海贫血特征
alpha thalassemia
α型地中海贫血
beta thalassemia
β型地中海贫血
thalassemia screening
地中海贫血筛查
thalassemia test
地中海贫血检测
thalassemia carrier
地中海贫血携带者
thalassemia diagnosis
地中海贫血诊断
thalassemia patient
地中海贫血患者
thalassemia is a hereditary blood disorder characterized by abnormal hemoglobin production.
地中海贫血是一种遗传性血液疾病，其特征是血红蛋白生成异常。
many people are unaware they carry the thalassemia gene until their child is diagnosed.
许多人直到孩子被确诊才知道自己携带地中海贫血基因。
regular blood transfusions are essential for patients with thalassemia major.
定期输血对地中海贫血重症患者至关重要。
prenatal screening can detect thalassemia in unborn babies with high accuracy.
产前筛查可以高准确度地检测胎儿是否患有地中海贫血。
iron overload is a serious complication that requires chelation therapy in thalassemia patients.
铁过载是一种严重的并发症，地中海贫血患者需要螯合治疗。
thalassemia carrier screening is recommended for couples planning to start a family.
建议计划组建家庭的夫妇进行地中海贫血携带者筛查。
the severity of thalassemia depends on how many mutated genes a person inherits.
地中海贫血的严重程度取决于一个人继承了多少突变基因。
advances in gene therapy offer new hope for curing thalassemia in the future.
基因治疗的进步为未来治愈地中海贫血带来了新的希望。
thalassemia intermedia patients experience moderate symptoms compared to the major form.
中间型地中海贫血患者的症状比重型患者轻微。
children with thalassemia major often require lifelong medical care and support.
重型地中海贫血儿童通常需要终身的医疗护理和支持。
genetic counseling helps families understand the risks of passing thalassemia to their children.
遗传咨询帮助家庭了解将地中海贫血遗传给孩子的风险。
thalassemia is most prevalent in mediterranean, african, and southeast asian populations.
地中海贫血在地中海、非洲和东南亚人群中最为普遍。
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