Genomics and Health in the Developing WorldDhavendra Kumar Genomics and Health in the Developing World provides detailed and comprehensive coverage of population structures, human genomics, and genome variation - with particular emphasis on medical and health issues - in the emerging economies and countries of the developing world. With sections dedicated to fundamentals of genetics and genomics, epidemiology of human disease, biomarkers, comparative genomics, developments in translational genomic medicine, current and future health strategies related to genetic disease, and pertinent legislative and social factors, this volume highlights the importance of utilizing genetics/genomics knowledge to promote and achieve optimal health in the developing world. Grouped by geographic region, the chapters in this volume address: - Inherited disorders in the developing world, including a thorough look at genetic disorders in minority groups of every continent - The progress of diagnostic laboratory genetic testing, prenatal screening, and genetic counseling worldwide - Rising ethical and legal concerns of medical genetics in the developing world - Social, cultural, and religious issues related to genetic diseases across continents Both timely and vastly informative, this book is a unique and comprehensive resource for genetists, clinicians, and public health professionals interested in the social, ethical, economic, and legal matters associated with medical genetics in the developing world. |
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ADPKD African populations allele analysis anemia Asia Asian association studies autosomal dominant autosomal recessive Beighton birth defects blood cancer cause chromosome Clin clinical common congenital consanguineous deafness developing countries developing world diagnosis drug dysplasia effect encoding enzyme ethnic factors falciparum fetal Founder effect frequency G6PD deficiency gene genetic disorders genetic testing genome-wide genomic genomic medicine genotype glaucoma global groups haplogroups haplotype healthcare hemochromatosis hemoglobin hepcidin hereditary heterozygous homozygous Hum Genet Human Genetics identified increased Indian individuals infection inherited Islamic linkage loci locus major malaria mapping markers Medical Genetics metabolism mitochondrial molecular mutations Nat Genet obesity patients Pharmacogenetics phenotype polycystic kidney disease polymorphisms prevalence protein receptor region renal disease reported result risk role Science screening sequence severe malaria sickle cell SNPs South Africa susceptibility syndrome technologies thalassemia therapy tion treatment tuberculosis Tunisia type 2 diabetes vaccines variants Weatherall