Technical, genetic, and ethical issues in screening and testing of African-Americans for hemochromatosis

被引:4
作者
Bowman, JE
机构
[1] Univ Chicago, Comm Genet, Dept Pathol, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Genet, Dept Med, Chicago, IL 60637 USA
[3] Univ Chicago, MacLean Ctr Clin Med Eth, Chicago, IL 60615 USA
来源
GENETIC TESTING | 2000年 / 4卷 / 02期
关键词
D O I
10.1089/10906570050114920
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To define more precisely populations in which hemochromatosis is frequent to rare, problems of racial classification are introduced, with particular reference to Europeans and African-Americans, Because the category "Caucasian" includes a multitude of dissimilar peoples, the categories Europeans and European-Americans have been substituted for Caucasian, which is archaic. The background of discrimination in sickle hemoglobin programs for African-Americans are then analyzed, including, discrimination by employers, life insurance, and selective mandatory testing. Discrimination and selective testing of African-American employees of the Lawrence Livermore Laboratory continues today without prior consent, as it has since the 1970s, Dissimilarities between the genetics of hemochromatosis in Europeans and their descendants, Africans, and African-Americans are briefly analyzed, Finally, it is concluded that because hemochromatosis is unlike sickle hemoglobin in that it is potentially preventable and treatable, prevention and treatment principles should apply as in other diseases. Furthermore, because hemochromatosis is so common in European-Americans, discrimination, if practiced, would not be selective for African-Americans.
引用
收藏
页码:207 / 212
页数:6
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