thalassemia major

A pair of twin girls suffered from thalassemia major.

一对孪生姐妹婴儿患上了重型地中海贫血。

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Genetic Study on 27 Children with β-thalassemia Major and Their Parents in Sichuan Area

四川地区重型β-地中海贫血患儿及双亲基因突变的研究

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MR imaging of femoral marrow in treated β-thalassemia major

经治重型β地中海贫血的股骨骨髓MR成像分析

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Change of Serum Ferritin Level in Hyper Transfusion Thalassemia Major Children Treated by Different Dosage of Iron Chelator

不同剂量铁螯合剂治疗高量输血重型β珠蛋白生成障碍贫血患儿血清铁蛋白的变化

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Most of dual gene mutations were thalassemia major, but also observed in a few of thalassemia minor cases.

β地贫基因突变以点突变为主，双重基因突变子多为重型β地贫，亦见于少数轻型β地贫。

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Applying the methods mentioned to diagnose the fetuses who are in the risk of thalassemia major in prenatal diagnosis can prevent the births of these babies. 3.

上述技术可应用于对重型地贫高风险胎儿的产前诊断，有效预防重型地中海贫血患儿出生。

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Prophylaxis of Transplantation-related Complications after Allogeneic Stem Cell Transplantation in β-thalassemia Major

儿童重型β-地中海贫血异基因造血干细胞移植后并发症的防治

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Prenatal diagnosis was carried out by the mentioned techniques above for fetuses who were in the risk of thalassemia major. 5.

将上述方法运用于重型地中海贫血高风险胎儿的产前诊断中。

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In 30 cases of thalassemia minor, there were 28 cases of gene mutation heterozygotes, 2 cases of which were dual gene mutations, and 5 cases of thalassemia major were all dual gene mutations.

30例轻型β地贫中，28例为基因突变杂合子，2例是双重基因突变子；5例重型β地贫中，均为基因双重突变子。

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Meta-analysis of the efficacy and safety of combined therapy with deferiprone and deferoxamine in thalassemia major patients

去铁酮和去铁胺治疗珠蛋白生成障碍性贫血临床疗效及安全性的Meta分析

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Objective To reduce the birthrate of β-thalassemia major and improve the quality of population.

目的为了降低β地中海贫血重症患儿的出生率，达到优生的目的。

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Twelve ( 8 males and 4 females) patients with β-thalassemia major received the hematological stem cell transplantation ( HSCT).

12例接受造血干细胞移植治疗的重型β地中海贫血患儿，年龄从25岁～115岁，男8例，女4例。

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Objective To reduce the birth rate of β-thalassemia major and improve the quality of population.

目的减少β-地中海贫血重症患儿的出生。

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Treatment of thalassemia major with unrelated donor bone marrow transplantation

非血缘相关骨髓移植治疗重型地中海贫血的临床研究

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α-Thalassemia major is a hereditary disease with a syndrome of hemolytic anemia, often caused bv the complete or partial deletion of a-globin genes.

α-地中海贫血是由于α-珠蛋白基因全部和部分缺失所致的一种遗传性溶血性贫血综合征。

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Transplantation with Combination of Umbilical Cord Blood and Neonatal Peripheral Blood in the Treatment of A Patient with β-thalassemia Major

脐带血、新生儿外周血混合移植治疗1例重型β-地中海贫血

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Conclusions It suggests that the PCR-RDB assay is effective in preventing the birth of β-thalassemia major and has clinical significance in improving the population quality.

结论PCR-RDB技术可有效减少β地中海贫血重症患儿的出生，具有重要的优生学意义。

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Objective To investigate the change of serum ferritin ( SF) level in hyper transfusion thalassemia major ( TM) children treated with different dosage of iron chelator.

目的探讨采用不同剂量铁螯合剂治疗高量输血重型β珠蛋白生成障碍贫血（地贫）患儿1年后的血清铁蛋白（SF）的变化。

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The purpose of this study was to designed to analyze and explore the diagnosis and treatment on a patient with β-thalassemia major accompanied with intestinal acute graft-versus-host disease ( aGVHD) grade ⅳ after allo-peripheral blood stem cell transplantation ( allo-PBSCT).

对1例异基因外周血干细胞移植（allo PBSCT）治疗重型β地中海贫血（TM）患儿合并Ⅳ度肠道aGVHD的诊断和治疗进行分析和探讨。

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Conclusion The results showed that Allo PBSCT was successful in treating β thalassemia major.

结论异基因外周血造血干细胞移植治疗重型β地贫患儿已获得成功。

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Umbilical cord blood transplantation for patients with β-thalassemia major

脐血移植治疗重型β地中海贫血的临床研究

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Multiple Regression Analysis of Liver Pathology and Other Factors in Children with β Thalassemia Major

重型β珠蛋白生成障碍性贫血肝脏病理与相关因素的多重回归分析

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