000 | 01411nam a22001937a 4500 | ||
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008 | 220616b2020 |||||||| |||| 00| 0 eng d | ||
020 | _a9780367702670 | ||
020 | _a9781138298392 | ||
060 | _aWH 170 | ||
100 | 1 | _aDyson, Simon | |
245 |
_aSickle cell and the social sciences : _bhealth, racism and disablement |
||
260 |
_aAbingdon : _bTaylor and Francis, _c2020 |
||
300 | _aix, 241p | ||
490 | _aRoutledge studies in the sociology of health and illness | ||
520 | _aSickle cell disease (SCD) is a severe chronic illness and one of the world's most common genetic conditions, with 400,000 children born annually with the disorder, mainly in Sub-Saharan Africa, India, Brazil, the Middle East and in diasporic African populations in North America and Europe. Biomedical treatments for SCD are increasingly available to the world's affluent populations, while such medical care is available only in attenuated forms in Africa, India and to socio-economically disadvantaged groups in North America and Europe. Tackling the controversial role of screening and genetics in SCD, the book offers a brief thematic history of approaches to the condition, queries the role of ethnicity and includes a discussion of how the social model of disability can be applied, as well as featuring chapters focusing on athletics, prisons and schools. | ||
650 | _aSickle cell | ||
650 | _aRace | ||
942 |
_n0 _01 |
||
999 |
_c78910 _d78910 |