Thalassemia 是 什么 - 地中海贫血会遗传吗?唯一避免重型地贫患儿出生的有效手段是……_腾讯新闻

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是 什么 thalassemia 地中海贫血是什么病?地中海贫血是什么病,怎么治疗 爱问知识人

地中海貧血

是 什么 thalassemia 地中海贫血是什么病?地中海贫血是什么病,怎么治疗 爱问知识人

什么是地中海贫血(Thalassemia Major)?

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是 什么 thalassemia Iron Chelators

乙型地中海型貧血 (Beta

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地中海贫血是什么病?地中海贫血是什么病,怎么治疗 爱问知识人

Reduced amounts of detectable beta globin causes beta-plus-thalassemia.

  • Clinically, beta-thalassemia is divided into thalassemia major which is transfusion dependent, thalassemia intermedia of intermediate severity , and thalassemia minor that is asymptomatic.

  • Chelators are small molecules that bind very tightly to metal ions.

flex属性

Others are complex proteins made by living organisms e.

  • Subcutaneous desferrioxamine: the effect of three years' treatment on liver, iron, serum ferritin, and comments on echocardiography.

  • Since each unit of blood deposits about 230 mg of iron, most patients who require, for instance, 2 units of blood per month will have at most a very slightly negative iron balance with chelation therapy.




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