The Enculturated Gene :Sickle Cell Health Politics and Biological Difference in West Africa

Publication subTitle :Sickle Cell Health Politics and Biological Difference in West Africa

Author: Fullwiley Duana  

Publisher: Princeton University Press‎

Publication year: 2011

E-ISBN: 9781400840410

P-ISBN(Paperback): 9780691123172

Subject: R556.6 hemolytic anemia

Keyword: 文化人类学、社会人类学,预防医学、卫生学,非洲史

Language: ENG

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Description

In the 1980s, a research team led by Parisian scientists identified several unique DNA sequences, or haplotypes, linked to sickle cell anemia in African populations. After casual observations of how patients managed this painful blood disorder, the researchers in question postulated that the Senegalese type was less severe. The Enculturated Gene traces how this genetic discourse has blotted from view the roles that Senegalese patients and doctors have played in making sickle cell "mild" in a social setting where public health priorities and economic austerity programs have forced people to improvise informal strategies of care.


Duana Fullwiley shows how geneticists, who were fixated on population differences, never investigated the various modalities of self-care that people developed in this context of biomedical scarcity, and how local doctors, confronted with dire cuts in Senegal's health sector, wittingly accepted the genetic prognosis of better-than-expected health outcomes. Unlike most genetic determinisms that highlight the absoluteness of disease, DNA haplotypes for sickle cell in Senegal did the opposite. As Fullwiley demonstrates, they allowed the condition to remain officially invisible, never to materialize as a health priority. At the same time, scientists' attribution of a less severe form of Senegalese sickle cell to isolated DNA sequences closed off other explanations of this population's measured biological success.



Th

Chapter

Two – Healthy Sicklers with “Mild” Disease: Local Illness Affects and Population-Level Effects

Three – The Biosocial Politics of Plants and People

Four – Attitudes of Care

Five – Localized Biologies: Mapping Race and Sickle Cell Difference in French West Africa

Six – Ordering Illness: Heterozygous “Trait” Suffering in the Land of the Mild Disease

Seven – The Work of Patient Advocacy

Conclusion – Economic and Health Futures amid Hope and Despair

Notes

References

Index

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