Objective To investigate whether alpha-thalassemia can be diagnosed with extraembryonic coelomic cells.
目讨胚外体腔穿刺术应用于α海贫血产前诊可行性。
To evaluate the safety and efficacy of combining deferiprone(DFP)and deferoxamine(DFO)in iron chelation therapy in patients with thalassemia.
讨去铁酮(DFP)和去铁胺(DFO)联合用药对重海贫血螯合治疗安全性和有效性。
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Usually, patients with mild thalassemia don’t need treatment, while patients with severe thalassemia are treated with blood transfusions.
通常情况下，地中海贫血无需治疗，而重地贫患者需输血治疗。
The initial symptoms of minor and moderate alpha thalassemia are due to anemia, which include pallor, shortness of breath, and easy fatigability.
中α地中海贫血的首发症状往往是贫血，表现为苍白、气促、乏力。
All right, as a quick recap: alpha thalassemia is an autosomal recessive disorder caused by deletion of alpha globin genes on chromosome 16.
得！快速回顾一下：α地中海贫血是一种常染色体隐性病，由16号染色体上的α珠蛋白基因缺陷引起。
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划词翻译
详细解释
讨胚外体腔穿刺术应用于α
海贫血产前诊
可行性。
地中海贫血无需治疗，而重
中
病，由16号染色体上的α珠蛋白基因缺陷引起。
