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全科及家庭医疗环境中的血红蛋白病

Hemoglobinopathies in a general and family practice setting.

作者信息

Carr C M, Chapatwala K D, Nandedkar A K

出版信息

J Natl Med Assoc. 1989 Feb;81(2):137-9.

PMID:2733052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2625969/
Abstract

The incidence of sickle cell trait varies among blacks in North America. Although the average hemoglobin (Hb)-AS gene frequency is 8% in the United States, a value of 13.4% was recorded in South Carolina. Preliminary studies during a two-day community sponsored health fair in Selma, Alabama, revealed a sickle cell gene frequency of 15.96%. This study also found an intermediate frequency of 12.4% in a family practice center that is accredited for a residency program. Through a screening program, sickle cell trait was detected, a rigorous training program for resident physicians in family practice was implemented, and proper counseling to patients with hemoglobinopathies was provided. In the authors' judgment, laboratory screening for sickle cell trait is a first step toward genetic counseling and medical practice by family physicians and general practitioners.

摘要

镰状细胞性状的发病率在北美黑人中各不相同。尽管在美国,血红蛋白(Hb)-AS基因的平均频率为8%,但在南卡罗来纳州记录的值为13.4%。在阿拉巴马州塞尔玛市为期两天的社区赞助健康博览会上进行的初步研究显示,镰状细胞基因频率为15.96%。该研究还在一个获得住院医师培训项目认证的家庭医疗中心发现了12.4%的中间频率。通过一项筛查计划,检测出了镰状细胞性状,为家庭医疗住院医师实施了严格的培训计划,并为血红蛋白病患者提供了适当的咨询。作者认为,对镰状细胞性状进行实验室筛查是家庭医生和全科医生进行遗传咨询和医疗实践的第一步。

相似文献

1
Hemoglobinopathies in a general and family practice setting.全科及家庭医疗环境中的血红蛋白病
J Natl Med Assoc. 1989 Feb;81(2):137-9.
2
Sickle gene frequency in a southcentral Alabama family medical program.阿拉巴马州中南部家庭医疗项目中的镰状基因频率
Ala Med. 1988 Oct;58(4):17-8.
3
Incidence of haemoglobinopathies detected through neonatal screening in the United Arab Emirates.阿拉伯联合酋长国通过新生儿筛查检测出的血红蛋白病发病率。
East Mediterr Health J. 2005 May;11(3):300-7.
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Genetic Blood Disorders Survey in the Sultanate of Oman.阿曼苏丹国的遗传性血液疾病调查。
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[Screening for hemoglobinopathies at a knowledge center in Copenhagen. Resources should be allocated to solve a growing health problem in the Nordic countries].[哥本哈根一个知识中心的血红蛋白病筛查。应分配资源以解决北欧国家日益严重的健康问题]
Lakartidningen. 2000 May 31;97(22):2752-4.
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Laboratory Diagnosis of sickling hemoglobinopathies.镰状血红蛋白病的实验室诊断
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Haemoglobin SD disease--rare case of jaundice.血红蛋白SD病——黄疸罕见病例。
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Screening for abnormal hemoglobins: who, when, and how.异常血红蛋白筛查:对象、时机与方法
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Successful newborn sickle cell trait counseling program using health department nurses.利用卫生部门护士开展成功的新生儿镰状细胞性状咨询项目。
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10
Laws in question: Confusion over sickle cell testing.相关法律:镰状细胞检测方面的混乱情况。
Hastings Cent Rep. 1972 Dec;3(1):3-4.

本文引用的文献

1
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Direct identification of sickle cell anemia by blot hybridization.通过印迹杂交直接鉴定镰状细胞贫血。
Proc Natl Acad Sci U S A. 1981 Aug;78(8):5081-5. doi: 10.1073/pnas.78.8.5081.
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Sickle cell anemia and related hemoglobinopathies.镰状细胞贫血及相关血红蛋白病
Pediatr Clin North Am. 1980 May;27(2):429-47. doi: 10.1016/s0031-3955(16)33860-3.
6
Identification of hemoglobins and hemoglobinopathies by electrophoresis on cellulose acetate plates impregnated with citrate agar.通过在浸有柠檬酸盐琼脂的醋酸纤维素板上进行电泳来鉴定血红蛋白和血红蛋白病。
Clin Chem. 1974;20(1):74-7.
7
Sickle-cell anemia and other hemoglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens.镰状细胞贫血及其他血红蛋白病。以滤纸上的血斑为标本进行筛查的程序和策略。
N Engl J Med. 1973 Jun 14;288(24):1265-8. doi: 10.1056/NEJM197306142882403.
8
Sickle cell anemia in two White American children: essential laboratory criteria for diagnosis.两名美国白人儿童的镰状细胞贫血:诊断的基本实验室标准。
Pediatrics. 1979 Feb;63(2):242-6.
9
Methods for detection of hemoglobin variants and hemoglobinopathies in the routine clinical laboratory.常规临床实验室中血红蛋白变异体和血红蛋白病的检测方法。
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