Hereditary Red Cell Disorders in Southeast Asian Refugees and the Effect on the Prevalence of Thalassemia Disorders in the United States
Hereditary Red Cell Disorders in Southeast Asian Refugees and the Effect on the Prevalence of Thalassemia Disorders in the United States
复制标题
东南亚难民的遗传性红细胞疾病及其对美国地中海贫血症患病率的影响
DOI：
10.1097/00000441-198609000-00005
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发表时间：
1986
期刊：
影响因子：
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通讯作者：
S. Elliot
中科院分区：
文献类型：
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作者：
C. Monzon;V. Fairbanks;E. Burgert;J. Sutherland;S. Elliot
本研究确定了一组东南亚个体中血红蛋白E、α和β地中海贫血以及葡萄糖-6-磷酸脱氢酶缺乏症的频率和患病率，并确定了其对美国地中海贫血疾病患病率的影响。东南亚难民的重新安置计划大大增加了美国严重地中海贫血症患者的总数。在几代人的时间里，东南亚儿童将是地中海贫血的主要群体。
This investigation established the frequency and prevalence of hemoglobin E, α and β thalassemia, and glucose-6-phosphate dehydrogenase deficiency in a group of Southeast Asian individuals and determined the impact upon the prevalence of thalassemia disorders in the United States. The resettlement program of Southeast Asian refugees has significantly increased the total number of serious thalassemic disorders in the United States. For several generations Southeast Asian children will be the principal thalassemic group.
DOI：
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发表时间：
1981
期刊：
Clinics in haematology
影响因子：
--
作者：
Wasi,P
通讯作者：
Wasi,P