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Health Disparities: Sickle Cell, Research and CRISPR
Date
September 27, 2018
Free
Standard Price
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About 100,000 people in the United States have sickle cell disease, with most of the patient population derived from communities of African descent. While life expectancy for almost every major disease or chronic condition is improving, patients with sickle cell disease can expect to die younger than they did 20 years ago. In 1994, life expectancy for sickle cell patients was 42 for men and 48 for women. By 2005, life expectancy had dipped to 38 for men and 42 for women.
Gene editing offers the potential to find therapies for life-threatening and/or debilitating human genetic diseases – from cardiac and metabolic diseases, to neurological diseases such as Huntington’s disease, to sickle cell anemia. Yet human gene editing raises many questions related to bioethics and equity.
This session centers on the intersection of scientific research and public policy to eliminate health disparities, we will seek to answer:
Why we are moving in the wrong direction in terms of life expectancy?
What are the barriers to care?
Who can access these therapies?
How is personal choice given a fair voice?
Who funds a cure?
Keystone Symposia is striving to advance understanding and elimination of persistent health disparities in the United States by incorporating discussion into our conferences on cardiovascular and metabolic diseases, immunology, cancer, and other diseases that impact populations worldwide.
The pharmaceutical industry needs access to innovation from academia to develop new drugs, and academic institutions are more interested than ever in finding a commercial route for their discoveries…
_GENOMIC VARIATION IS A DRIVING FORCE IN DETERMINING ANIMAL AND HUMAN HEALTH AND SUSCEPTIBILITY TO DISEASE._ Animal breeding has made huge strides in optimizing yield while lowering costs, and lessening the impact on the environment while also improving the general health of the animals…
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