Status and Management of Sickle Cell Disease among Nilgiri Tribes. Este artículo no está disponible.
Idioma: inglés
Editorial: LAP LAMBERT Academic Publishing, 2017
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- Nuevo

Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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Vendedor de IberLibro desde 6 de enero de 2003
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EUR 105,19
Descripción del artículo del vendedor
100 pages. 8.66x5.91x0.23 inches. In Stock.
N° de ref. del artículo __3659813818
- Título
- Status and Management of Sickle Cell Disease among Nilgiri Tribes
- Autor
- Marimuthu, Prashanthi Devi/ Balan, Brindha
- Editorial
- LAP LAMBERT Academic Publishing
- Año de publicación
- 2017
- Estado
- Brand New
- Encuadernación
- Paperback
- Idioma
- inglés
- ISBN 10
- 3659813818
- ISBN 13
- 9783659813818
- Peso del artículo
- 0,2 kilogramos
Sickle cell disease (SCD) is the most prevalent inherited blood condition worldwide resulting from single DNA mutation within the beta globin gene. About 20 per cent of children with sickle disease die by the age of two in India as reported by ICMR survey, and 30 per cent children with SCD among the tribal community die before they reach adulthood. The disease poses an economical and psychological burden on the affected individual, family and society as a whole. Management strategies has been designed to improve the quality of life of most vulnerable tribes such as Irulas, Kurumbas and Paniyans especially those in the age group of 25-49 and 0-14. This book places suggestions and recommendations for policy makers to revise the health care policy so as to accommodate the tribal illness or diseases in the National Health Policy in a more effective manner so as to improve the quality of lives of people living with sickle-cell anaemia in the Nilgiris District of India.
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Reseña del editor
Sickle cell disease (SCD) is the most prevalent inherited blood condition worldwide resulting from single DNA mutation within the beta globin gene. About 20 per cent of children with sickle disease die by the age of two in India as reported by ICMR survey, and 30 per cent children with SCD among the tribal community die before they reach adulthood. The disease poses an economical and psychological burden on the affected individual, family and society as a whole. Management strategies has been designed to improve the quality of life of most vulnerable tribes such as Irulas, Kurumbas and Paniyans especially those in the age group of 25-49 and 0-14. This book places suggestions and recommendations for policy makers to revise the health care policy so as to accommodate the tribal illness or diseases in the National Health Policy in a more effective manner so as to improve the quality of lives of people living with sickle-cell anaemia in the Nilgiris District of India.
“Acerca de” puede pertenecer a otra edición de este título.